Multi-layer golf ball with reaction injection molded polyurethane component

ABSTRACT

Disclosed herein is a multi-layer golf ball having a soft outer cover. The golf ball has a core, one or more mantle or inner cover layers with a Shore D hardness of 60 or more, and an outer cover with a Shore D hardness of 53 or less. In a particularly preferred form of the invention, the inner and/or outer cover layers comprise a reaction injection molded polyurethane. The golf ball of the invention has exceptionally soft feel and high spin rates on short shots of 80 yards or less and, particularly, 40 yards or less, while maintaining good distance and average spin on full shots.

CROSS REFERENCES TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 09/610,416 filed on Jul. 5, 2000 now U.S. Pat. No. 6,663,508, which is a continuation-in-part of U.S. application Ser. No. 09/387,953 filed Sep. 1, 1999, now U.S. Pat. No. 6,287,217, which is a divisional of U.S. application Ser. No. 09/040,887 filed Mar. 18, 1998, now U.S. Pat. No. 6,083,119, which is a continuation-in-part of U.S. application Ser. No. 08/631,613 filed Apr. 10, 1996, now U.S. Pat. No. 5,803,831, which is a continuation-in-part of (1) U.S. application Ser. No. 08/591,046 filed on Jan. 25, 1996 now abandoned; and (2) U.S. application Ser. No. 08/542,793 filed on Oct. 13, 1995 now abandoned, which is a continuation-in-part of U.S. application Ser. No. 08/070,510 filed Jun. 1, 1993, now abandoned.

FIELD OF THE INVENTION

The present invention relates to golf balls and, more particularly, to improved golf balls comprising multi-layer covers which have a hard inner layer and a relatively soft outer layer. In a preferred embodiment, the present invention golf balls utilize outer covers formed from reaction injection molded polyurethane.

BACKGROUND OF THE INVENTION

Traditional golf ball covers have been comprised of balata or blends of balata with elastomeric or plastic materials. The traditional balata covers are relatively soft and flexible. Upon impact, the soft balata covers compress against the surface of the club producing high spin. Consequently, the soft and flexible balata covers provide an experienced golfer with the ability to apply a spin to control the ball in flight in order to produce a draw or a fade, or a backspin which causes the ball to “bite” or stop abruptly on contact with the green. Moreover, the soft balata covers produce a soft “feel” to the low handicap player. Such playability properties (workability, feel, etc.) are particularly important in short iron play with low swing speeds and are exploited significantly by relatively skilled players.

Despite all the benefits of balata, balata covered golf balls are easily cut and/or damaged if mis-hit. Golf balls produced with balata or balata-containing cover compositions therefore have a relatively short lifespan.

As a result of this negative property, balata and its synthetic substitutes, transpolybutadiene and transpolyisoprene, have been essentially replaced as the cover materials of choice by new cover materials comprising ionomeric resins.

Ionomeric resins are polymers containing interchain ionic bonding. As a result of their toughness, durability and flight characteristics, various ionomeric resins sold by E. I. DuPont de Nemours & Company under the trademark “Surlyn®” and more recently, by the Exxon Corporation (see U.S. Pat. No. 4,911,451) under the trademarks “ESCOR®” and the trade name “lotek,” have become the materials of choice for the construction of golf ball covers over the traditional “balata” (transpolyisoprene, natural or synthetic) rubbers. As stated, the softer balata covers, although exhibiting enhanced playability properties, lack the durability (cut and abrasion resistance, fatigue endurance, etc.) properties required for repetitive play.

Ionomeric resins are generally ionic copolymers of an olefin, such as ethylene, and a metal salt of an unsaturated carboxylic acid, such as acrylic acid, methacrylic acid, or maleic acid. Metal ions, such as sodium or zinc, are used to neutralize some portion of the acidic group in the copolymer resulting in a thermoplastic elastomer exhibiting enhanced properties, i.e. durability, etc., for golf ball cover construction over balata. However, some of the advantages gained in increased durability have been offset to some degree by the decreases produced in playability. This is because although the ionomeric resins are very durable, they tend to be very hard when utilized for golf ball cover construction, and thus lack the degree of softness required to impart the spin necessary to control the ball in flight. Since the ionomeric resins are harder than balata, the ionomeric resin covers do not compress as much against the face of the club upon impact, thereby producing less spin. In addition, the harder and more durable ionomeric resins lack the “feel” characteristic associated with the softer balata related covers.

As a result, while there are currently more than fifty (50) commercial grades of ionomers available both from DuPont and Exxon, with a wide range of properties which vary according to the type and amount of metal cations, molecular weight, composition of the base resin (i.e., relative content of ethylene and methacrylic and/or acrylic acid groups) and additive ingredients such as reinforcement agents, etc., a great deal of research continues in order to develop a golf ball cover composition exhibiting not only the improved impact resistance and carrying distance properties produced by the “hard” ionomeric resins, but also the playability (i.e., “spin,” “feel,” etc.) characteristics previously associated with the “soft” balata covers, properties which are still desired by the more skilled golfer.

Consequently, a number of two-piece (a solid resilient center or core with a molded cover) and three-piece (a liquid or solid center, elastomeric winding about the center, and a molded cover) golf balls have been produced to address these needs. The different types of materials utilized to formulate the cores, covers, etc. of these balls dramatically alters the balls' overall characteristics. In addition, multi-layered covers containing one or more ionomer resins have also been formulated in an attempt to produce a golf ball having the overall distance, playability and durability characteristics desired.

This was addressed by Spalding Sports Worldwide, Inc., the assignee of the present invention, in U.S. Pat. No. 4,431,193 where a multilayered golf ball is produced by initially molding a first cover layer on a spherical core and then adding a second layer. The first layer is comprised of a hard, high flexural modulus resinous material such as type 1605 Surlyn® (now designated Surlyn® 8940). Type 1605 Surlyn (Surlyn® 8940) is a sodium ion based low acid (less than or equal to 15 weight percent methacrylic acid) ionomer resin having a flexural modulus of about 51,000 psi. An outer layer of a comparatively soft, low flexural modulus resinous material such as type 1855 Surlyn® (now designated Surlyn® 9020) is molded over the inner cover layer. Type 1855 Surlyn® (Surlyn® 9020) is a zinc ion based low acid (10 weight percent methacrylic acid) ionomer resin having a flexural modulus of about 14,000 psi.

The '193 patent teaches that the hard, high flexural modulus resin which comprises the first layer provides for a gain in coefficient of restitution over the coefficient of restitution of the core. The increase in the coefficient of restitution provides a ball which serves to attain or approach the maximum initial velocity limit of 255 feet per second as provided by the United States Golf Association (U.S.G.A.) rules. The relatively soft, low flexural modulus outer layer provides for the advantageous “feel” and playing characteristics of a balata covered golf ball.

In various attempts to produce a durable, high spin ionomer golf ball, the golfing industry has blended the hard ionomer resins with a number of softer ionomeric resins. U.S. Pat. Nos. 4,884,814 and 5,120,791 are directed to cover compositions containing blends of hard and soft ionomeric resins. The hard copolymers typically are made from an olefin and an unsaturated carboxylic acid. The soft copolymers are generally made from an olefin, an unsaturated carboxylic acid, and an acrylate ester. It has been found that golf ball covers formed from hard-soft ionomer blends tend to become scuffed more readily than covers made of hard ionomer alone. It would be useful to develop a golf ball having a combination of softness and durability which is better than the softness-durability combination of a golf ball cover made from a hard-soft ionomer blend.

Most professional golfers and good amateur golfers desire a golf ball that provides distance when hit off a driver, control and stopping ability on full iron shots, and high spin on short “touch and feel” shots. Many conventional two-piece and thread wound performance golf balls have undesirable high spin rates on full shots. The excessive spin on full shots is a sacrifice made in order to achieve more spin which is desired on the shorter touch shots. It would be beneficial to provide a golf ball which has high spin for touch shots without generating excessive spin on full shots.

An object of the invention is to provide a golf ball with a soft cover which has good scuff resistance.

Yet another object of the invention is to provide a golf ball having a favorable combination of spin rate and durability.

A further object of the invention is to provide a golf ball having a soft cover made from a cover material which is blended with minimal mixing difficulties.

Another object of the invention is to provide a method of making a golf ball which has a soft cover with good scuff resistance and cut resistance.

Another object of the invention is to provide a golf ball which has a high spin on shots of 250 feet or less and an average spin on full shots using a 9 iron.

Yet another object of the invention is to provide a method of making a durable golf ball with a relatively high spin rate.

A further object of the invention is to provide a multi-layer golf ball having exceptionally soft feel and high spin rates on short shots while maintaining good distance on full shots.

Yet another object of the invention is to provide a multi-layer golf ball having a high spin rate on short shots and not having an excessive spin rate on long shots.

A significant object of the present invention is to provide a golf ball having an inner component such as a mantle layer or an outer cover layer that is formed from a reaction injection method (RIM) from one or more polyurethanes.

Other objects will be in part obvious and in part pointed out more in detail hereafter.

SUMMARY OF THE INVENTION

The present invention provides, in a first aspect, a golf ball comprising a core, a mantle layer or inner cover layer formed about the core, and an outer cover layer disposed on the inner cover layer. The inner cover layer is relatively hard, having a Shore D hardness of at least 60. The outer cover layer is relatively soft, having a Shore D hardness of less than 53. And, the outer cover layer comprises a reaction injection molded polyurethane.

In another aspect, the present invention provides a golf ball comprising a core, a mantle layer formed about the core, and an outer cover layer formed over the mantle layer. The outer cover has a Shore D hardness of no more than 53. The outer cover layer comprises a polyurethane. The resulting golf ball exhibits a PGA compression of 100 or less and a coefficient of restitution of at least 0.750.

In yet another embodiment, the present invention provides a method of forming a golf ball. The method comprises providing a core, positioning the core in a molding chamber, and then forming a mantle layer about the core. The method further comprises forming a cover layer on the mantle via a reaction injection molding technique.

The invention accordingly comprises the several steps and the relation of one or more of such steps with respect to each of the others and the article possessing the features, properties, and the relation of elements exemplified in the following detailed disclosure.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a cross-sectional view of a golf ball embodying the invention illustrating a core 10 and a cover 12 consisting of an inner layer 14 and an outer layer 16 having dimples 18;

FIG. 2 is a diametrical cross-sectional view of a golf ball of the invention having a core 10 and a cover 12 made of an inner layer 14 and an outer layer 16 having dimples 18;

FIG. 3 is a process flow diagram which schematically depicts a reaction injection molding process according to the invention;

FIG. 4 schematically shows a mold for reaction injection molding a golf ball cover according to the invention; and

FIG. 5 illustrates a cross-sectional view of another preferred embodiment golf ball in accordance with the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The invention in a preferred form is a golf ball comprising a core, a mantle or inner cover layer formed about the core, the inner cover layer having a Shore D hardness of at least 60 as measured on the curved surface thereof, and an outer cover layer formed over the inner cover layer, the outer cover layer having a Shore D hardness of no more than 53 as measured on the curved surface thereof. Preferably, at least one of the mantle or inner cover layer and the outer cover layer comprises reaction-injection-molded polyurethanes. The golf ball exhibits a PGA compression of 100 or less and a coefficient of restitution of at least 0.750. The outer cover layer preferably has a Shore D hardness of no more than 50. The outer cover layer preferably has a Shore D hardness of 30–50. The outer cover layer preferably has a Shore D hardness of 45–53 as measured on the curved surface thereof. The ball preferably has a PGA compression of 90 or less.

The mantle or inner cover layer preferably has a Shore D hardness of 60–85, and more preferably 65–85. The inner cover layer preferably has a Shore D hardness of 60–85 as measured on the curved surface thereof.

The golf ball of the invention preferably has a core which is a solid or is filled with liquid. The core can be wound or non-wound. A wound core may comprise a liquid, solid, gel or multi-piece center. In one preferred form of the invention, at least one of the inner and outer cover layers has a thickness of 0.01–0.150 inches, more preferably 0.02–0.10 inches, and even more preferably 0.03–0.07 inches.

Yet another preferred form of the invention is a golf ball comprising a core, a mantle layer or an inner cover layer formed from a composition which includes at least 50 weight percent reaction-injection-molded polyurethanes, and an outer cover layer formed over the inner cover layer, the outer cover layer having a Shore D hardness of no more than 53 as measured on the curved surface thereof, the golf ball having a PGA compression of 100 or less and a coefficient of restitution of at least 0.750.

In yet another preferred form of the invention, a golf ball is provided that comprises a core, a mantle layer disposed about the core, and one or more cover layers disposed about the mantle layers. At least one of the mantle and cover layers are formed from a composition that includes at least one or more polyurethanes. Preferably, the composition includes at least 50 weight percent reaction injection molded polyurethanes. It is most preferred that the mantle comprise polyurethane and be formed via a reaction injection molding technique.

Referring to FIGS. 1 and 2, the present invention relates to improved multi-layer golf balls, particularly a golf ball comprising a multi-layered cover 12 over a core 10, and method for making same. The golf balls of the invention, which can be of a standard or enlarged size, have a unique combination of high coefficient of restitution and a high spin rate on short shots.

The core 10 of the golf ball can be formed of a solid, a liquid, or any other substance which will result in an inner ball, i.e. core and inner cover layer, having the desired COR, compression and hardness. The multi-layered cover 12 comprises two layers: a first or inner layer or ply 14 and a second or outer layer or ply 16. The inner layer 14 can be ionomer, ionomer blends, non-ionomer, non-ionomer blends, or blends of ionomer and non-ionomer. The outer layer 16 is softer than the inner layer and can be ionomer, ionomer blends, non-ionomer, non-ionomer blends or blends of ionomer and non-ionomer.

In a first preferred embodiment, the inner layer 14 is comprised of a high acid (i.e. greater than 16 weight percent acid) ionomer resin or high acid ionomer blend. Preferably, the inner layer is comprised of a blend of two or more high acid (i.e., at least 16 weight percent acid) ionomer resins neutralized to various extents by different metal cations. The inner cover layer may or may not include a metal stearate (e.g., zinc stearate) or other metal fatty acid salt. The purpose of the metal stearate or other metal fatty acid salt is to lower the cost of production without affecting the overall performance of the finished golf ball. In a second embodiment, the inner layer 14 is comprised of a low acid (i.e. 16 weight percent acid or less) ionomer blend. Preferably, the inner layer is comprised of a blend of two or more low acid (i.e. 16 weight percent acid or less) ionomer resins neutralized to various extents by different metal cations. The inner cover layer may or may not include a metal stearate (e.g., zinc stearate) or other metal fatty acid salt. The purpose of the metal stearate or other metal fatty acid salt is to lower the cost of production without affecting the overall performance of the finished golf ball.

FIG. 5 illustrates another preferred embodiment golf ball 20 in accordance with the present invention. This preferred ball 20 comprises a core 22, at least one mantle layer 24, or inner cover layer 26 disposed about the core 22, and an outermost cover layer 28. One or more of the cover layers comprise polyurethane and are formed by a RIM process. These aspects are described in greater detail herein.

It has been found that a hard inner layer provides for a substantial increase in resilience (i.e., enhanced distance) over known multi-layer covered balls. The softer outer layer provides for desirable “feel” and high spin rate while maintaining respectable resiliency. The soft outer layer allows the cover to deform more during impact and increases the area of contact between the club face and the cover, thereby imparting more spin on the ball. As a result, the soft cover provides the ball with a balata-like feel and playability characteristics with improved distance and durability. Consequently, the overall combination of the inner and outer cover layers results in a golf ball having enhanced resilience (improved travel distance) and durability (i.e., cut resistance, etc.) characteristics while maintaining and in many instances, improving the playability properties of the ball.

The combination of a hard inner cover layer with a soft, relatively low modulus ionomer, ionomer blend or other non-ionomeric thermoplastic elastomer outer cover layer provides for excellent overall coefficient of restitution (i.e., excellent resilience) because of the improved resiliency produced by the inner cover layer. While some improvement in resiliency is also produced by the outer cover layer, the outer cover layer generally provides for a more desirable feel and high spin, particularly at lower swing speeds with highly lofted clubs such as half wedge shots.

Inner Cover Layer

The inner cover layer is harder than the outer cover layer and generally has a thickness in the range of 0.01 to 0.150 inches, preferably 0.02 to 0.10 inches, and more preferably 0.03 to 0.06 inches for a 1.68 inch ball and 0.03 to 0.07 inches for a 1.72 inch (or more) ball. The core and inner cover layer together form an inner ball preferably having a coefficient of restitution of 0.770 or more and more preferably 0.780 or more, and a diameter in the range of 1.48–1.66 inches for a 1.68 inch ball and 1.50–1.70 inches for a 1.72 inch (or more) ball. The inner cover layer has a Shore D hardness of 60 or more. It is particularly advantageous if the golf balls of the invention have an inner layer with a Shore D hardness of 65 or more. The above-described characteristics of the inner cover layer preferably provide an inner ball having a PGA compression of 100 or less. It is found that when the inner ball has a PGA compression of 90 or less, excellent playability results.

The inner layer compositions may utilize the high acid ionomers such as those developed by E. I. DuPont de Nemours & Company under the trademark “Surlyn®” and by Exxon Corporation under the trademark “Escor®” or tradename “lotek”, or blends thereof. Examples of compositions which may be used as the inner layer herein are set forth in detail in a continuation of U.S. application Ser. No. 08/174,765, which is a continuation of U.S. Ser. No. 07/776,803 filed Oct. 15, 1991, and Ser. No. 08/493,089, which is a continuation of Ser. No. 07/981,751, which in turn is a continuation of Ser. No. 07/901,660 filed Jun. 19, 1992, incorporated herein by reference. Of course, the inner layer high acid ionomer compositions are not limited in any way to those compositions set forth in said copending applications.

The high acid ionomers which may be suitable for use in formulating the inner layer compositions are ionic copolymers which are the metal, i.e., sodium, zinc, magnesium, etc., salts of the reaction product of an olefin having from about 2 to 8 carbon atoms and an unsaturated monocarboxylic acid having from about 3 to 8 carbon atoms. Preferably, the ionomeric resins are copolymers of ethylene and either acrylic or methacrylic acid. In some circumstances, an additional comonomer such as an acrylate ester (i.e., iso- or n-butylacrylate, etc.) can also be included to produce a softer terpolymer. The carboxylic acid groups of the copolymer are partially neutralized (i.e., approximately 10–100%, preferably 30–70%) by the metal ions. Each of the high acid ionomer resins which may be included in the inner layer cover compositions of the invention contains greater than about 16% by weight of a carboxylic acid, preferably from about 17% to about 25% by weight of a carboxylic acid, more preferably from about 18.5% to about 21.5% by weight of a carboxylic acid.

Although the inner layer cover composition preferably includes a high acid ionomeric resin and the scope of the patent embraces all known high acid ionomeric resins falling within the parameters set forth above, only a relatively limited number of these high acid ionomeric resins have recently become commercially available.

The high acid ionomeric resins available from Exxon under the designation “Escor®)” and or “lotek”, are somewhat similar to the high acid ionomeric resins available under the “Surlyn®” trademark. However, since the Escor®/lotek ionomeric resins are sodium or zinc salts of poly(ethylene-acrylic acid) and the “Surlyn®” resins are zinc, sodium, magnesium, etc. salts of poly(ethylene-methacrylic acid), distinct differences in properties exist.

Examples of the high acid methacrylic acid based ionomers found suitable for use in accordance with this invention include Surlyn®8220 and 8240 (both formerly known as forms of Surlyn AD-8422), Surlyn®9220 (zinc cation), Surlyn® SEP-503-1 (zinc cation), and Surlyn®SEP-503-2 (magnesium cation). According to DuPont, all of these ionomers contain from about 18.5 to about 21.5% by weight methacrylic acid.

More particularly, Surlyn® AD-8422 is currently commercially available from DuPont in a number of different grades (i.e., AD-8422-2, AD-8422-3, AD-8422-5, etc.) based upon differences in melt index. According to DuPont, Surlyn® 8422, which is believed recently to have been redesignated as 8220 and 8240, offers the following general properties when compared to Surlyn® 8920, the stiffest, hardest of all on the low acid grades (referred to as “hard” ionomers in U.S. Pat. No. 4,884,814):

TABLE 1 LOW ACID (15 wt % HIGH ACID Acid) (>20 wt % Acid) SURLYN ® SURLYN ® SURLYN ® 8920 8422-2 8422-3 IONOMER Cation Na Na Na Melt Index 1.2 2.8 1.0 Sodium, Wt % 2.3 1.9 2.4 Base Resin MI 60 60 60 MP¹, ° C. 88 86 85 FP¹, ° C. 47 48.5 45 COMPRESSION MOLDING² Tensile Break, psi 4350 4190 5330 Yield, psi 2880 3670 3590 Elongation, % 315 263 289 Flex Mod, K psi 53.2 76.4 88.3 Shore D 66 67 68 hardness ¹DSC second heat, 10° C./min heating rate. ²Samples compression molded at 150° C. annealed 24 hours at 60° C. 8422-2, -3 were homogenized at 190° C. before molding.

In comparing Surlyn® 8920 to Surlyn® 8422-2 and Surlyn® 8422-3, it is noted that the high acid Surlyn® 8422-2 and 8422-3 ionomers have a higher tensile yield, lower elongation, slightly higher Shore D hardness and much higher flexural modulus. Surlyn® 8920 contains 15 weight percent methacrylic acid and is 59% neutralized with sodium.

In addition, Surlyn®SEP-503-1 (zinc cation) and Surlyn® SEP-503-2 (magnesium cation) are high acid zinc and magnesium versions of the Surlyn® AD 8422 high acid ionomers. When compared to the Surlyn® AD 8422 high acid ionomers, the Surlyn® SEP-503-1 and SEP-503-2 ionomers can be defined as follows:

Surlyn ® Ionomer Ion Melt Index Neutralization % AD 8422-3 Na 1.0 45 SEP 503-1 Zn 0.8 38 SEP 503-2 Mg 1.8 43

Furthermore, Surlyn® 8162 is a zinc cation ionomer resin containing approximately 20% by weight (i.e., 18.5–21.5% weight) methacrylic acid copolymer that has been 30–70% neutralized. Surlyn® 8162 is currently commercially available from DuPont.

Examples of the high acid acrylic acid based ionomers suitable for use in the present invention also include the Escor® or lotek high acid ethylene acrylic acid ionomers produced by Exxon such as Ex 1001, 1002, 959, 960, 989, 990, 1003, 1004, 993, 994. In this regard, Escor® or lotek 959 is a sodium ion neutralized ethylene-acrylic neutralized ethylene-acrylic acid copolymer. According to Exxon, loteks 959 and 960 contain from about 19.0 to 21.0% by weight acrylic acid with approximately 30 to about 70 percent of the acid groups neutralized with sodium and zinc ions, respectively. The physical properties of these high acid acrylic acid based ionomers are as follows:

TABLE 2 Exxon High Acid Ionomers ESCOR ® ESCOR ® (IOTEK) (IOTEK) PROPERTY Ex 1001 Ex 1002 959 Ex 1003 Ex 1004 960 Melt index, 1.0 1.6 2.1 1.1 2.0 1.8 g/10 min Cation Na Na Na Zn Zn Zn Melting 83.7 83.7 — 82 82.5 79 Point, ° C. Vicat 51.5 51.5 58 56 55 55 Softening Point, ° C. Tensile @ Break 34.4 MPa 31.7 MPa  34 MPa 24.8 MPa 20.6 MPa  24 MPa Elongation @ Break, % 341 348 280 387 437 430 Hardness, 63 62 65 54 53 57 Shore D Flexural  365 MPa  380 MPa 480 MPa  147 MPa  130 Mpa 170 MPa Modulus

TABLE 3 Additional Exxon High Acid Ionomers Property Unit EX 989 EX 993 EX 994 EX 990 Melt index g/10 min 1.30 1.25 1.32 1.24 Moisture ppm 482 214 997 654 Cation type — Na Li K Zn M+ content by AAS wt % 2.74 0.87 4.54 0 Zn content by AAS wt % 0 0 0 3.16 Density kg/m³ 959 945 976 977 Vicat softening point ° C. 52.5 51 50 55.0 Crystallization point ° C. 40.1 39.8 44.9 54.4 Melting point ° C. 82.6 81.0 80.4 81.0 Tensile at yield MPa 23.8 24.6 22 16.5 Tensile at break MPa 32.3 31.1 29.7 23.8 Elongation at break % 330 260 340 357 1% secant modulus MPa 389 379 312 205 Flexural modulus MPa 340 368 303 183 Abrasion resistance mg 20.0 9.2 15.2 20.5 Hardness Shore D — 62 62.5 61 56 Zwick Rebound % 61 63 59 48

Furthermore, as a result of the development by the assignee of this application of a number of new high acid ionomers neutralized to various extents by several different types of metal cations, such as by manganese, lithium, potassium, calcium and nickel cations, several new high acid ionomers and/or high acid ionomer blends besides sodium, zinc and magnesium high acid ionomers or ionomer blends are now available for golf ball cover production. It has been found that these new cation neutralized high acid ionomer blends produce inner cover layer compositions exhibiting enhanced hardness and resilience due to synergies which occur during processing. Consequently, the metal cation neutralized high acid ionomer resins recently produced can be blended to produce substantially higher C.O.R.'s than those produced by the low acid ionomer inner cover compositions presently commercially available.

More particularly, several new metal cation neutralized high acid ionomer resins have been produced by the inventor by neutralizing, to various extents, high acid copolymers of an alpha-olefin and an alpha, beta-unsaturated carboxylic acid with a wide variety of different metal cation salts. This discovery is the subject matter of U.S. application Ser. No. 08/493,089, incorporated herein by reference. It has been found that numerous new metal cation neutralized high acid ionomer resins can be obtained by reacting a high acid copolymer (i.e., a copolymer containing greater than 16% by weight acid, preferably from about 17 to about 25 weight percent acid, and more preferably about 20 weight percent acid), with a metal cation salt capable of ionizing or neutralizing the copolymer to the extent desired (i.e., from about 10% to 90%).

The base copolymer is made up of greater than 16% by weight of an alpha, beta-unsaturated carboxylic acid and an alpha-olefin. Optionally, a softening comonomer can be included in the copolymer. Generally, the alpha-olefin has from 2 to 10 carbon atoms and is preferably ethylene, and the unsaturated carboxylic acid is a carboxylic acid having from about 3 to 8 carbons. Examples of such acids include acrylic acid, methacrylic acid, ethacrylic acid, chloroacrylic acid, crotonic acid, maleic acid, fumaric acid, and itaconic acid, with acrylic acid being preferred.

The softening comonomer that can be optionally included in the inner cover layer for the golf ball of the invention may be selected from the group consisting of vinyl esters of aliphatic carboxylic acids wherein the acids have 2 to 10 carbon atoms, vinyl ethers wherein the alkyl groups contains 1 to 10 carbon atoms, and alkyl acrylates or methacrylates wherein the alkyl group contains 1 to 10 carbon atoms. Suitable softening comonomers include vinyl acetate, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl acrylate, butyl methacrylate, or the like.

Consequently, examples of a number of copolymers suitable for use to produce the high acid ionomers included in the present invention include, but are not limited to, high acid embodiments of an ethylene/acrylic acid copolymer, an ethylene/methacrylic acid copolymer, an ethylene/itaconic acid copolymer, an ethylene/maleic acid copolymer, an ethylene/methacrylic acid/vinyl acetate copolymer, an ethylene/acrylic acid/vinyl alcohol copolymer, etc. The base copolymer broadly contains greater than 16% by weight unsaturated carboxylic acid, from about 39 to about 83% by weight ethylene and from 0 to about 40% by weight of a softening comonomer. Preferably, the copolymer contains about 20% by weight unsaturated carboxylic acid and about 80% by weight ethylene. Most preferably, the copolymer contains about 20% acrylic acid with the remainder being ethylene.

Along these lines, examples of the preferred high acid base copolymers which fulfill the criteria set forth above, are a series of ethylene-acrylic copolymers which are commercially available from The Dow Chemical Company, Midland, Mich., under the “Primacor” designation. These high acid base copolymers exhibit the typical properties set forth below in Table 4.

TABLE 4 Typical Properties of Primacor Ethylene-Acrylic Acid Copolymers MELT TENSILE FLEXURAL VICAT PERCENT DENSITY, INDEX, YD. ST MODULUS SOFT PT SHORE D GRADE ACID glcc g/10 min (psi) (psi) (° C.) HARDNESS ASTM D-792 D-1238* D-638 D-790 D-1525 D-2240 5980 20.0 0.958  300.0 — 4800 43 50 5990 20.0 0.955 1300.0 650 2600 40 42 5981 20.0 0.960  300.0 900 3200 46 48 5983 20.0 0.958  500.0 850 3100 44 45 5991 20.0 0.953 2600.0 635 2600 38 40 *190° C.

Due to the high molecular weight of the Primacor 5981 grade of the ethylene-acrylic acid copolymer, this copolymer is the more preferred grade utilized in the invention.

The metal cation salts utilized in the invention are those salts which provide the metal cations capable of neutralizing, to various extents, the carboxylic acid groups of the high acid copolymer. These include acetate, oxide or hydroxide salts of lithium, calcium, zinc, sodium, potassium, nickel, magnesium, and manganese.

Examples of such lithium ion sources are lithium hydroxide monohydrate, lithium hydroxide, lithium oxide and lithium acetate. Sources for the calcium ion include calcium hydroxide, calcium acetate and calcium oxide. Suitable zinc ion sources are zinc acetate dihydrate and zinc acetate, a blend of zinc oxide and acetic acid. Examples of sodium ion sources are sodium hydroxide and sodium acetate. Sources for the potassium ion include potassium hydroxide and potassium acetate. Suitable nickel ion sources are nickel acetate, nickel oxide and nickel hydroxide. Sources of magnesium include magnesium oxide, magnesium hydroxide, magnesium acetate. Sources of manganese include manganese acetate and manganese oxide.

The new metal cation neutralized high acid ionomer resins are produced by reacting the high acid base copolymer with various amounts of the metal cation salts above the crystalline melting point of the copolymer, such as at a temperature from about 200° F. to about 500° F., preferably from about 250° F. to about 350° F. under high shear conditions at a pressure of from about 10 psi to 10,000 psi. Other well known blending techniques may also be used. The amount of metal cation salt utilized to produce the new metal cation neutralized high acid based ionomer resins is the quantity which provides a sufficient amount of the metal cations to neutralize the desired percentage of the carboxylic acid groups in the high acid copolymer. The extent of neutralization is generally from about 10% to about 90%.

As indicated below in Table 5 and more specifically in Example 1 in U.S. application Ser. No. 08/493,089, a number of new types of metal cation neutralized high acid ionomers can be obtained from the above indicated process. These include new high acid ionomer resins neutralized to various extents with manganese, lithium, potassium, calcium and nickel cations. In addition, when a high acid ethylene/acrylic acid copolymer is utilized as the base copolymer component of the invention and this component is subsequently neutralized to various extents with the metal cation salts producing acrylic acid based high acid ionomer resins neutralized with cations such as sodium, potassium, lithium, zinc, magnesium, manganese, calcium and nickel, several new cation neutralized acrylic acid based high acid ionomer resins are produced.

TABLE 5 Formulation Wt-% Wt-% Melt Shore D No. Cation Salt Neutralization Index C.O.R. Hardness  1(NaOH) 6.98 67.5 0.9 .804 71  2(NaOH) 5.66 54.0 2.4 .808 73  3(NaOH) 3.84 35.9 12.2 .812 69  4(NaOH) 2.91 27.0 17.5 .812 (brittle)  5(MnAc) 19.6 71.7 7.5 .809 73  6(MnAc) 23.1 88.3 3.5 .814 77  7(MnAc) 15.3 53.0 7.5 .810 72  8(MnAc) 26.5 106 0.7 .813 (brittle)  9(LiOH) 4.54 71.3 0.6 .810 74 10(LiOH) 3.38 52.5 4.2 .818 72 11(LiOH) 2.34 35.9 18.6 .815 72 12(KOH) 5.30 36.0 19.3 Broke 70 13(KOH) 8.26 57.9 7.18 .804 70 14(KOH) 10.7 77.0 4.3 .801 67 15(ZnAc) 17.9 71.5 0.2 .806 71 16(ZnAc) 13.9 53.0 0.9 .797 69 17(ZnAc) 9.91 36.1 3.4 .793 67 18(MgAc) 17.4 70.7 2.8 .814 74 19(MgAc) 20.6 87.1 1.5 .815 76 20(MgAc) 13.8 53.8 4.1 .814 74 21(CaAc) 13.2 69.2 1.1 .813 74 22(CaAc) 7.12 34.9 10.1 .808 70 23(MgO) 2.91 53.5 2.5 .813 24(MgO) 3.85 71.5 2.8 .808 25(MgO) 4.76 89.3 1.1 .809 26(MgO) 1.96 35.7 7.5 .815 27(NiAc) 13.04 61.1 0.2 .802 71 28(NiAc) 10.71 48.9 0.5 .799 72 29(NiAc) 8.26 36.7 1.8 .796 69 30(NiAc) 5.66 24.4 7.5 .786 64 Controls: 50/50 Blend of Ioteks 8000/7030 C.O.R. = .810/65 Shore D Hardness DuPont High Acid Surlyn ® 8422 (Na) C.O.R. = .811/70 Shore D Hardness DuPont High Acid Surlyn ® 8162 (Zn) C.O.R. = .807/65 Shore D Hardness Exxon High Acid Iotek EX-960 (Zn) C.O.R. = .796/65 Shore D Hardness Control for Formulations 23–26 is 50/50 Iotek 8000/7030, C.O.R. = .814, Formulation 26 C.O.R. was normalized to that control accordingly Control for Formulation Nos. 27–30 is 50/50 Iotek 8000/7030, C.O.R. = .807 When compared to low acid versions of similar cation neutralized ionomer resins, the new metal cation neutralized high acid ionomer resins exhibit enhanced hardness, modulus and resilience characteristics. These are properties that are particularly desirable in a number of thermoplastic fields, including the field of golf ball manufacturing.

When utilized in the construction of the inner layer of a multilayered golf ball, it has been found that the new acrylic acid based high acid ionomers extend the range of hardness beyond that previously obtainable while maintaining the beneficial properties (i.e. durability, click, feel, etc.) of the softer low acid ionomer covered balls, such as balls produced utilizing the low acid ionomers disclosed in U.S. Pat. Nos. 4,884,814 and 4,911,451.

Moreover, as a result of the development of a number of new acrylic acid based high acid ionomer resins neutralized to various extents by several different types of metal cations, such as manganese, lithium, potassium, calcium and nickel cations, several new ionomers or ionomer blends are now available for production of an inner cover layer of a multi-layered golf ball. By using these high acid ionomer resins, harder, stiffer inner cover layers having higher C.O.R.s, and thus longer distance, can be obtained.

More preferably, it has been found that when two or more of the above-indicated high acid ionomers, particularly blends of sodium and zinc high acid ionomers, are processed to produce the covers of multi-layered golf balls, (i.e., the inner cover layer herein) the resulting golf balls will travel further than previously known multi-layered golf balls produced with low acid ionomer resin covers due to the balls' enhanced coefficient of restitution values.

The low acid ionomers which may be suitable for use in formulating the inner layer compositions of the second and third embodiments of the subject invention are ionic copolymers which are the metal, i.e., sodium, zinc, magnesium, etc., salts of the reaction product of an olefin having from about 2 to 8 carbon atoms and an unsaturated monocarboxylic acid having from about 3 to 8 carbon atoms. Preferably, the ionomeric resins are copolymers of ethylene and either acrylic or methacrylic acid. In some circumstances, an additional comonomer such as an acrylate ester (i.e., iso- or n-butylacrylate, etc.) can also be included to produce a softer terpolymer. The carboxylic acid groups of the copolymer are partially neutralized (i.e., approximately 10–100%, preferably 30–70%) by the metal ions. Each of the low acid ionomer resins which may be included in the inner layer cover compositions of the invention contains 16% by weight or less of a carboxylic acid.

The inner layer compositions include the low acid ionomers such as those developed and sold by E.I. DuPont de Nemours & Company under the trademark “Surlyn®” and by Exxon Corporation under the trademark “Escor®” or tradename “lotek,” or blends thereof.

The low acid ionomer resins available from Exxon under the designation “Escor®” and/or “lotek,” are somewhat similar to the low acid ionomeric resins available under the “Surlyn®” trademark. However, since the Escor®/lotek ionomeric resins are sodium or zinc salts of poly(ethylene-acrylic acid) and the “Surlyn®” resins are zinc, sodium, magnesium, etc. salts of poly(ethylene-methacrylic acid), distinct differences in properties exist.

When utilized in the construction of the inner layer of a multilayered golf ball, it has been found that the low acid ionomer blends extend the range of compression and spin rates beyond that previously obtainable. More preferably, it has been found that when two or more low acid ionomers, particularly blends of sodium and zinc ionomers, are processed to produce the covers of multi-layered golf balls, (i.e., the inner cover layer herein) the resulting golf balls will travel further and at an enhanced spin rate than previously known multi-layered golf balls. Such an improvement is particularly noticeable in enlarged or oversized golf balls.

As shown in the Examples, use of an inner layer formulated from blends of lower acid ionomers produces multi-layer golf balls having enhanced compression and spin rates. These are the properties desired by the more skilled golfer.

In a particularly preferred embodiment of the inner cover layer, a blend of high and low acid ionomer resins is used. These can be the ionomer resins described above, combined in a weight ratio which preferably is within the range of 10–90 to 90–10 high and low acid ionomer resins.

Another embodiment of the inner cover layer is primarily or fully non-ionomeric thermoplastic material. Suitable non-ionomeric materials include metallocene catalyzed polyolefins or polyamides, polyamide/ionomer blends, polycarbonates, polyphenylene ether/ionomer blends, etc., which has a Shore D hardness of ≧60 and preferably have a flex modulus of greater than about 30,000 psi, or other hardness and flex modulus values which are comparable to the properties of the ionomers described above. Other suitable materials include but are not limited to thermoplastic or thermosetting polyurethanes/polyureas, including castable polyurethanes/polyureas, reaction injection moldable polyurethanes/polyureas, thermoplastic block polyesters, such as a polyester elastomer marketed by DuPont under the trademark Hytrel®, thermoplastic block polyamides, such as a polyester amide marked by Elf Atochem S.A. under the trademark Pebax®, a blend of two or more non-ionomeric thermoplastic elastomers, or a blend of one or more ionomers and one or more non-ionomeric thermoplastic elastomers. These materials can be blended with the ionomers described above in order to reduce cost relative to the use of higher quantities of ionomer.

A preferred embodiment golf ball of the present invention comprises one or more inner cover layers disposed about a core. For example, mantle or inner cover layer 24 is depicted in FIG. 5. The thickness of a mantle layer is generally governed by the thicknesses and weights of other components in a golf ball, namely the core and cover layer(s). The mantle layer generally comprises one or more of the materials or compositions described herein for the outer cover layer.

The preferred composition for the inner cover layer may comprise up to 100 weight percent of a non-ionomeric thermoplastic or thermoset material including a thermoplastic polyester polyurethane such as B.F. Goodrich Company's Estane® polyester polyurethane X-4517 or a reaction-injection molded material such as one or more of the Bayflex RIM polyurethanes from Bayer. The non-ionomeric thermoplastic material may be blended with a soft ionomer. For example, polyamides blend well with soft ionomer. According to B.F. Goodrich, Estane® X-4517 has the following properties as set forth in Table 6:

TABLE 6 Properties of Estane ® X-4517 Tensile 1430 100%  815 200% 1024 300% 1193 Elongation  641 Youngs Modulus 1826 Hardness A/D 88/39 Bayshore Rebound  59 Solubility in Water Insoluble Melt processing temperature >350° F. (>177° C.) Specific Gravity (H₂O = 1) 1.1–1.3

Other soft, relatively low modulus non-ionomeric thermoplastic or thermoset materials may also be utilized to produce the preferred mantle layer as long as the non-ionomeric materials produce the playability and durability characteristics desired without adversely affecting the enhanced travel distance characteristic produced by the high acid ionomer resin composition. These include, but are not limited to thermoplastic polyurethanes such as Texin thermoplastic polyurethanes from Mobay Chemical Co. and the Pellethane thermoplastic polyurethanes from Dow Chemical Co.; non-ionomeric thermoset polyurethanes including but not limited to those disclosed in U.S. Pat. No. 5,334,673; cross-linked metallocene catalyzed polyolefins; ionomer/rubber blends such as those in Spalding U.S. Pat. Nos. 4,986,545; 5,098,105 and 5,187,013; and, styrene-butadiene-styrene block copolymers, including functionalized styrene-butadiene-styrene block copolymers, styrene-ethylene-butadiene-styrene (SEBS) block copolymers such as KRATON materials from Shell Chemical Co., including functionalized SEBS block copolymers; and, Hytrel polyester elastomers from DuPont and Pebax polyesteramides from Elf Atochem S.A.

Notwithstanding the foregoing, the preferred embodiment is to utilize a reaction injection molded (RIM) polyurethane mantle as described herein. RIM is a process by which highly reactive liquids are injected into a closed mold, mixed usually by impingement and/or mechanical mixing in an in-line device such as a “peanut mixer”, where they polymerize primarily in the mold to form a coherent, one-piece molded article. The RIM processes usually involve a rapid reaction between one or more reactive components such as polyether- or polyester-polyol, polyamine, or other material with an active hydrogen, and one or more isocyanate—containing constituents, often in the presence of a catalyst. The constituents are stored in separate tanks prior to molding and may be first mixed in a mix head upstream of a mold and then injected into the mold. The liquid streams are metered in the desired weight to weight ratio and fed into an impingement mix head, with mixing occurring under high pressure, e.g., 1500 to 3000 psi. The liquid streams impinge upon each other in the mixing chamber of the mix head and the mixture is injected into the mold. One of the liquid streams typically contains a catalyst for the reaction. The constituents react rapidly after mixing to gel and form polyurethane polymers. Polyureas, epoxies, and various unsaturated polyesters also can be molded by RIM.

RIM differs from non-reaction injection molding in a number of ways. The main distinction is that in RIM a chemical reaction takes place in the mold to transform a monomer or adducts to polymers and the components are in liquid form. Thus, a RIM mold need not be made to withstand the pressures which occur in a conventional injection molding. In contrast, injection molding is conducted at high molding pressures in the mold cavity by melting a solid resin and conveying it into a mold, with the molten resin often being at about 150 to about 350° C. At this elevated temperature, the viscosity of the molten resin usually is in the range of 50,000 to about 1,000,000 centipoise, and is typically around 200,000 centipoise. In an injection molding process, the solidification of the resins occurs after about 10 to about 90 seconds, depending upon the size of the molded product, the temperature and heat transfer conditions, and the hardness of the injection molded material. Subsequently, the molded product is removed from the mold. There is no significant chemical reaction taking place in an injection molding process when the thermoplastic resin is introduced into the mold. In contrast, in a RIM process, the chemical reaction causes the material to set, typically in less than about 5 minutes, often in less than 2 minutes, preferably less than 1 minute, more preferably in less than 30 seconds, and in many cases in about 10 seconds or less.

If plastic products are produced by combining components that are preformed to some extent, subsequent failure can occur at a location on the component, e.g. the mantle layer, which is along the seam or parting line of the mold. Failure can occur at this location because this interfacial region is intrinsically different from the remainder of the component or layer and can be weaker or more stressed. The present invention is believed to provide for improved durability of a golf ball mantle layer by providing a uniform or “seamless” mantle in which the properties of the mantle material in the region along the parting line are generally the same as the properties of the mantle material at other locations on the mantle, including at the poles. The improvement in durability is believed to be a result of the fact that the reaction mixture is distributed uniformly into a closed mold. This uniform distribution of the injected materials substantially eliminates knit-lines and other molding deficiencies which can be caused by temperature difference and/or reaction difference in the injected materials. The process of the invention results in generally uniform molecular structure, density and stress distribution as compared to conventional injection-molding processes.

The most preferred commercially available polyurethane material for forming golf ball mantles in accordance with the present invention is Bayflex MP-10,000 system from Bayer Corporation of Pittsburgh, Pa. Although the Bayflex MP-10,000 two component polyurethane system is purported to be proprietary, the following information is available, set forth below-in Tables 7 and 8.

Details of Bayflex Component A are as follows in Table 7:

TABLE 7 CHEMICAL PRODUCT IDENTIFICATION PRODUCT NAME Bayflex MP-10,000 Component A PRODUCT CODE U-118-A CHEMICAL FAMILY Aromatic Isocyanate Prepolymer CHEMICAL NAME Diphenylmethane Diisocyanate (MDI) Prepolymer SYNONYMS Modified Diphenylmethane Diisocyanate (MDI) CAS NUMBER 3920-98-9 FORMULA Not Applicable PHYSICAL FORM Liquid COLOR Colorless to Straw Yellow MOLECULAR WEIGHT Average 600–700 BOILING POINT 406 F. (208 C.) @ 5 mmEg for MDI MELTIN/FREEZING POINT Range 59 F. (15 C.) to 68 F. (20 C.) SOLUBILITY IN WATER Reacts slowly with water to liberate CO₂ gas. SPECIFIC GRAVITY 1.21 @ 77 f (25 C.) BULK DENSITY 10.1 lbs/gal % VOLATILE BY VOLUME Negligible VAPOR PRESSURE Less than 10–5 mm Hg @ 77 F. (25 C.) for MDI VAPOR DENSITY 8.5 (MDI) (Air = 1)

Details of Bayflex Component B are as follows in Table 8:

TABLE 8 CHEMICAL PRODUCT IDENTIFICATION PRODUCT NAME Bayflex MP-10,000 Clear Component B PRODUCT CODE U-131-B CHEMICAL FAMILY Polyether Polyol System CHEMICAL NAME Polyether Polyol System containing Aromatic Diamine PHYSICAL AND CHEMICAL PROPERTIES PHYSICAL FORM Liquid COLOR Light Brown ODOR Slight amine odor ODOR THRESHOLD Not Established pH Not Established BOILING POINT Not Established MELTING/FREEZING Not Established POINT SOLUBILITY IN Complete WATER SPECIFIC GRAVITY 1.03 @ 77 F. (25 C.) BULK DENSITY 8.59 lbs/gal % VOLATILE BY Negligible VOLUME VAPOR PRESSURE Not Established VAPOR DENSITY Not Established (Air = 1)

Additional non-limiting examples of suitable RIM systems for use in the present invention are Bayflex® elastomeric polyurethane RIM systems, Baydur® GS solid polyurethane RIM systems, Prism® solid polyurethane RIM systems, all from Bayer Corp. (Pittsburgh, Pa.), SPECTRIM reaction moldable polyurethane and polyurea systems from Dow Chemical USA (Midland, Mich.), including SPECTRIM MM 373-A (isocyanate) and 373-B (polyol), and Elastolit SR systems from BASF (Parsippany, N.J.). Preferred RIM systems include Bayflex® MP-10,000 and Bayflex® 110-50, filled and unfilled. Further preferred examples are polyols, polyamines and isocyanates formed by processes for recycling polyurethanes and polyureas.

Outer Cover Layer

While the core with the hard inner cover layer formed thereon, provides the multi-layer golf ball with power and distance, the outer cover layer 16 is comparatively softer than the inner cover layer. The softness provides for the feel and playability characteristics typically associated with balata or balata-blend balls. The outer cover layer or ply is comprised of a relatively soft, low modulus (about 1,000 psi to about 10,000 psi) and, in one embodiment, low acid (less than 16 weight percent acid) ionomer, an ionomer blend, a non-ionomeric thermoplastic or thermosetting material such as, but not limited to, a metallocene catalyzed polyolefin such as EXACT material available from EXXON, a thermoplastic or thermoset polyurethanelpolyurea, including castable polyurethanes/polyureas, reaction injection moldable polyurethanes/polyureas, and injection moldable polyurethanes/polyureas, polycarbonates, thermoplastic block polyesters, such as a polyester elastomer marketed by DuPont under the trademark Hytrel®), thermoplastic block polyamides, such as a polyester amide marketed by Elf Atochem S.A. under the trademark Pebax®, a blend of two or more non-ionomeric thermoplastic or thermosetting materials, or a blend of one or more ionomers and one or more non-ionomeric thermoplastic materials.

The outer layer is preferably from about 0.010 to about 0.150 inches in thickness, more preferably 0.02–0.10 inches, more desirably 0.03 to 0.06 inches in thickness for a 1.680 inch ball and 0.03 to 0.07 inches in thickness for a 1.72 inch or more ball), but thick enough to achieve desired playability characteristics while minimizing expense. Thickness is defined as the average thickness of the non-dimpled areas of the outer cover layer. The outer cover layer 16 has a Shore D hardness of 55 or less, and more preferably 53 or less, and even more preferably 50 or less.

In one embodiment, the outer cover layer preferably is formed from an ionomer which constitutes at least 75 weight % of an acrylate ester-containing ionic copolymer or blend of acrylate ester-containing ionic copolymers. This type of outer cover layer in combination with the core and inner cover layer described above results in golf ball covers having a favorable combination of durability and spin rate. The one or more acrylate ester-containing ionic copolymers each contain an olefin, an acrylate ester, and an acid. In a blend of two or more acrylate ester-containing ionic copolymers, each copolymer may contain the same or a different olefin, acrylate ester and acid than are contained in the other copolymers. Preferably, the acrylate ester-containing ionic copolymer or copolymers are terpolymers, but additional monomers can be combined into the copolymers if the monomers do not substantially reduce the scuff resistance or other good playability properties of the cover.

For a given copolymer, the olefin is selected from the group consisting of olefins having 2 to 8 carbon atoms, including, as non-limiting examples, ethylene, propylene, butene-1, hexene-1 and the like. Preferably the olefin is ethylene.

The acrylate ester is an unsaturated monomer having from 1 to 21 carbon atoms which serves as a softening comonomer. The acrylate ester preferably is methyl, ethyl, n-propyl, n-butyl, n-octyl, 2-ethylhexyl, or 2-methoxyethyl 1-acrylate, and most preferably is methyl acrylate or n-butyl acrylate. Another suitable type of softening comonomer is an alkyl vinyl ether selected from the group consisting of n-butyl, n-hexyl, 2-ethylhexyl, and 2-methoxyethyl vinyl ethers.

The acid is a mono- or dicarboxylic acid and preferably is selected from the group consisting of methacrylic, acrylic, ethacrylic, α-chloroacrylic, crotonic, maleic, fumaric, and itaconic acid, or the like, and half esters of maleic, fumaric and itaconic acid, or the like. The acid group of the copolymer is 10–100% neutralized with any suitable cation, for example, zinc, sodium, magnesium, lithium, potassium, calcium, manganese, nickel, chromium, tin, aluminum, or the like. It has been found that particularly good results are obtained when the neutralization level is about 50–100%.

The one or more acrylate ester-containing ionic copolymers each has an individual Shore D hardness of about 5–64. The overall Shore D hardness of the outer cover is 55 or less, and generally is 40–55. It is preferred that the overall Shore D hardness of the outer cover is in the range of 40–50 in order to impart particularly good playability characteristics to the ball.

The outer cover layer of the invention is formed over a core or some underlying layer to result in a golf ball having a coefficient of restitution of at least 0.770, more preferably at least 0.780, and most preferably at least 0.790. The coefficient of restitution of the ball will depend upon the properties of both the core and the cover. The PGA compression of the golf ball is 100 or less, and preferably is 90 or less.

The acrylate ester-containing ionic copolymer or copolymers used in the outer cover layer can be obtained by neutralizing commercially available acrylate ester-containing acid copolymers such as polyethylene-methyl acrylate-acrylic acid terpolymers, including ESCOR ATX (Exxon Chemical Company) or poly (ethylene-butyl acrylate-methacrylic acid) terpolymers, including NUCREL (DuPont Chemical Company). Particularly preferred commercially available materials include ATX 320, ATX 325, ATX 310, ATX 350, and blends of these materials with NUCREL 010 and NUCREL 035. The acid groups of these materials and blends are neutralized with one or more of various cation salts including zinc, sodium, magnesium, lithium, potassium, calcium, manganese, nickel, etc. The degree of neutralization ranges from 10–100%. Generally, a higher degree of neutralization results in a harder and tougher cover material. The properties of non-limiting examples of commercially available un-neutralized acid terpolymers which can be used to form the golf ball outer cover layers of the invention are provided below in Table 9.

TABLE 9 Melt Index Flex Modulus dg/min Acid No. Mpa Hardness Trade Name ASTM D 1238 % KOH/g ASTM D790 (Shore D) ATX 310 6 45 80 44 ATX 320 5 45 50 34 ATX 325 20 45 9 30 ATX 350 6 15 20 28 Nucrel 010 11 60 40 40 Nucrel 035 35 60 59 40

The ionomer resins used to form the outer cover layers can be produced by reacting the acrylate ester-containing acid copolymer with various amounts of the metal cation salts at a temperature above the crystalline melting point of the copolymer, such as a temperature from about 200° F. to about 500° F., preferably from about 250° F. to about 350° F., under high shear conditions at a pressure of from about 100 psi to 10,000 psi. Other well known blending techniques may also be used. The amount of metal cation salt utilized to produce the neutralized ionic copolymers is the quantity which provides a sufficient amount of the metal cations to neutralize the desired percentage of the carboxylic acid groups in the high acid copolymer. When two or more different copolymers are to be used, the copolymers can be blended before or after neutralization. Generally, it is preferable to blend the copolymers before they are neutralized to provide for optimal mixing.

The compatibility of the acrylate ester-containing copolymers with each other in a copolymer blend produces a golf ball outer cover layer having a surprisingly good scuff resistance for a given hardness of the outer cover layer. The golf ball according to the invention has a scuff resistance of no higher than 3.0. It is preferred that the golf ball has a scuff resistance of no higher than about 2.5 to ensure that the golf ball is scuff resistant when used in conjunction with a variety of types of clubs, including sharp-grooved irons, which are particularly inclined to result in scuffing of golf ball covers. The best results according to the invention are obtained when the outer cover layer has a scuff resistance of no more than about 2.0. The scuff resistance test is described in detail below.

Additional materials may also be added to the inner and outer cover layer of the present invention as long as they do not substantially reduce the playability properties of the ball. Such materials include dyes (for example, Ultramarine Blue sold by Whitaker, Clark, and Daniels of South Plainsfield, N.J.) (see U.S. Pat. No. 4,679,795), pigments such as titanium dioxide, zinc oxide, barium sulfate and zinc sulfate; UV absorbers; antioxidants; antistatic agents; and stabilizers. Moreover, the cover compositions of the present invention may also contain softening agents such as those disclosed in U.S. Pat. Nos. 5,312,857 and 5,306,760, including plasticizers, metal stearates, processing acids, etc., and reinforcing materials such as glass fibers and inorganic fillers, as long as the desired properties produced by the golf ball covers of the invention are not impaired.

The outer layer in another embodiment of the invention includes a blend of a soft (low acid) ionomer resin with a small amount of a hard (high acid) ionomer resin. A low modulus ionomer suitable for use in the outer layer blend has a flexural modulus measuring from about 1,000 to about 10,000 psi, with a hardness of about 20 to about 40 on the Shore D scale. A high modulus ionomer herein is one which measures from about 15,000 to about 70,000 psi as measured in accordance with ASTM method D-790. The hardness may be defined as at least 50 on the Shore D scale as measured in accordance with ASTM method D-2240.

Soft ionomers primarily are used in formulating the hard/soft blends of the cover compositions. These ionomers include acrylic acid and methacrylic acid based soft ionomers. They are generally characterized as comprising sodium, zinc, or other mono- or divalent metal cation salts of a terpolymer of an olefin having from about 2 to 8 carbon atoms, methacrylic acid, acrylic acid, or another, α, β-unsaturated carboxylic acid, and an unsaturated monomer of the acrylate ester class having from 1 to 21 carbon atoms. The soft ionomer is preferably made from an acrylic acid base polymer is an unsaturated monomer of the acrylate ester class.

Certain ethylene-acrylic acid based soft ionomer resins developed by the Exxon Corporation under the designation “lotek 7520” (referred to experimentally by differences in neutralization and melt indexes as LDX 195, LDX 196, LDX 218 and LDX 219) may be combined with known hard ionomers such as those indicated above to produce the inner and outer cover layers. The combination produces higher C.O.R.s at equal or softer hardness, higher melt flow (which corresponds to improved, more efficient molding, i.e., fewer rejects) as well as significant cost savings versus the outer layer of multi-layer balls produced by other known hard-soft ionomer blends as a result of the lower overall raw materials cost and improved yields.

Test data collected by the inventors indicates that lotek 7520 resins have Shore D hardnesses of about 32 to 36 (per ASTM D-2240), melt flow indexes of 3±0.5 g/10 min (at 190° C. per ASTM D-1288), and a flexural modulus of about 2500–3500 psi (per ASTM D-790). Furthermore, testing by an independent testing laboratory by pyrolysis mass spectrometry indicates at lotek 7520 resins are generally zinc salts of a terpolymer of ethylene, acrylic acid, and methyl acrylate.

Furthermore, the inventors have found that a grade of an acrylic acid based soft ionomer available from the Exxon Corporation under the designation lotek 7510 is also effective when combined with the hard ionomers indicated above in producing golf ball covers exhibiting higher C.O.R. values at equal or softer hardness than those produced by known hard-soft ionomer blends. In this regard, lotek 7510 has the advantages (i.e. improved flow, higher C.O.R. values at equal hardness, increased clarity, etc.) produced by the lotek 7520 resin when compared to the methacrylic acid base soft ionomers known in the art (such as the Surlyn® 8625 and Surlyn® 8629 combinations disclosed in U.S. Pat. No. 4,884,814).

In addition, lotek 7510, when compared to lotek 7520, produces slightly higher C.O.R. values at equal softness/hardness due to the lotek 7510's higher hardness and neutralization. Similarly, lotek 7510 produces better release properties (from the mold cavities) due to its slightly higher stiffness and lower flow rate than lotek 7520. This is important in production where the soft covered balls tend to have lower yields caused by sticking in the molds and subsequent punched pin marks from the knockouts.

According to Exxon, lotek 7510 is of similar chemical composition as lotek 7520 (i.e. a zinc salt of a terpolymer of ethylene, acrylic acid, and methyl acrylate) but is more highly neutralized. Based upon FTIR analysis, lotek 7520 is estimated to be about 30–40 wt.-% neutralized and lotek 7510 is estimated to be about 40–60 wt.-% neutralized. The typical properties of lotek 7510 in comparison of those of lotek 7520 in comparison of those of lotek 7520 are set forth below.

TABLE 10 Physical Properties of Iotek 7510 in Comparison to Iotek 7520 Property Unit IOTEK 7520 IOTEK 7510 Melt Index g/10 min. 2.0 0.8 Density g/cc 0.96 0.97 Melting Point ° F. 151 149 Vicat softening point ° F. 108 109 Flex Modulus psi 3800 5300 Tensile Strength psi 1450 1750 Elongation % 760 690 Hardness, Shore D — 32 35

The hard ionomer resins utilized to produce the outer cover layer composition hard/soft blends include ionic copolymers which are the sodium, zinc, magnesium, lithium, etc. salts of the reaction product of an olefin having from 2 to 8 carbon atoms and an unsaturated monocarboxylic acid having from 3 to 8 carbon atoms. The carboxylic acid groups of the copolymer may be totally or partially (i.e. approximately 15–75 percent) neutralized.

The hard ionomeric resins are likely copolymers of ethylene and acrylic and/or methacrylic acid, with copolymers of ethylene and acrylic acid being the most preferred. Two or more types of hard ionomeric resins may be blended into the outer cover layer compositions in order to produce the desired properties of the resulting golf balls.

As discussed earlier herein, the hard ionomeric resins introduced under the designation Escor®) and sold under the designation “lotek” are somewhat similar to the hard ionomeric resins sold under the Surlyn® trademark. However, since the “lotek” ionomeric resins are sodium or zinc salts of poly(ethylene-acrylic acid) and the Surlyn® resins are zinc or sodium salts of poly(ethylene-methacrylic acid) some distinct differences in properties exist. As more specifically indicated in the data set forth below, the hard “lotek” resins (i.e., the acrylic acid based hard ionomer resins) are the more preferred hard resins for use in formulating the outer layer blends for use in the present invention. In addition, various blends of “lotek” and Surlyn® hard ionomeric resins, as well as other available ionomeric resins, may be utilized in the present invention in a similar manner.

Examples of commercially available hard ionomeric resins which may be used in the present invention in formulating the outer cover blends include the hard sodium ionic copolymer sold under the trademark Surlyn® 8940 and the hard zinc ionic copolymer sold under the trademark Surlyn® 9910. Surlyn® 8940 is a copolymer of ethylene with methacrylic acid and about 15 weight percent acid which is about 29 percent neutralized with sodium ions. This resin has an average melt flow index of about 2.8. Surlyn® 9910 is a copolymer of ethylene and methacrylic acid with about 15 weight percent acid which is about 58 percent neutralized with zinc ions. The average melt flow index of Surlyn® 9910 is about 0.7. The typical properties of Surlyn® 9910 and 8940, as well as other Surlyn® resins, are set forth below in Tables 11 and 12:

TABLE 11 Typical Properties of Commercially Available Hard Surlyn ® Resins Suitable for Use in the Outer Layer Blends of the Present Invention ASTM D 8940 9910 8920 8528 9970 9730 Cation Type Sodium Zinc Sodium Sodium Zinc Zinc Melt flow index, D-1238 2.8 0.7 0.9 1.3 14.0 1.6 gms/10 min. Specific Gravity, D-792 0.95 0.97 0.95 0.94 0.95 0.95 g/cm³ Hardness, Shore D D-2240 66 64 66 60 62 63 Tensile Strength, D-638 (4.8)  (3.6)  (5.4)  (4.2)  (3.2)  (4.1)  (kpsi), MPa 33.1 24.8 37.2 29.0 22.0 28.0 Elongation, % D-638 470 290 350 450 460 460 Flexural Modulus, D-790 (51)   (48)   (55)   (32)   (28)   (30)   (kpsi) MPa 350 330 380 220 190 210 Tensile Impact (23° C.) D-1822S 1020 1020 865 1160 760 1240 KJ/m₂ (ft.-lbs./in²) (485)  (485)  (410)  (550)  (360)  (590)  Vicat Temperature, ° C. D-1525 63 62 58 73 61 73

TABLE 12 Properties of Additional Hard Surlyn ® Resins SURLYN ® SURLYN ® SURLYN ® IONOMER 8920 8140 9120 Cation Na Na Zn Melt Flow Index gms/10 0.9 2.6 1.3 min. MP ° C. 84 88 85 FP ° C. 52 49 50 Tensile Strength kpsi 5.4 5.0 3.8 Yield Strength kpsi 2.2 2.8 2.4 Elongation % 350 340 280 Flex Modulus kpsi 55 71 64 Shore D Hardness 66 70 69

Examples of the more pertinent acrylic acid based hard ionomer resin suitable for use in the cover compositions sold under the “lotek” tradename by the Exxon Corporation include lotek, but are not limited to, 8000, 8010, 8020, 8030, 7030, 7010, 7020, EX 1001-1009, lotek 959 and lotek 960, as well as the materials listed above on Tables 2 and 3. The typical properties of the remainder of these and other lotek ionomers suited for use in formulating the cover compositions are set forth below in Tables 13 and 14:

TABLE 13 Typical Properties of Iotek Ionomers ASTM Resin Properties Method Units 7010 7020 7030 8000 8020 8030 Cation type zinc zinc zinc sodium sodium sodium Melt index D-1238 g/10 min. 0.8 1.5 2.5 0.8 1.6 2.8 Density D-1505 kg/m³ 968 966 954 957 956 956 Melting Point D-3417 ° C. 83.5 84 85 83 84 87 Crystallization Point D-3417 ° C. 55 56 58 45 47 49 Vicat Softening Point D-1525 ° C. 60 60 60 54 54.5 55.5 Tensile strength at D-638  MPA 24.5 23.5 22.6 33 32.5 32 break Yield strength D-638  MPA 14 13 12 19 18.5 18 Elongation at break D-638  % 440 450 460 370 380 410 1% Secant modulus D-638  MPA 150 135 125 280 280 280 Shore Hardness D D-2240 — 54 53 52 60 60 60 Flex modulus (3 mm) D-790  MPA 190 175 155 320 340 355

TABLE 14 Examples of Exxon High Molecular Weight Ionomers PROPERTY Ex1005 Ex1006 Ex1007 Ex1008 Ex1009 7310 Melt Index, g/10 min. 0.7 1.3 1.0 1.4 0.8 1.0 Cation Na Na Zn Zn Na Zn Melting Point, ° C. 85.3 86 85.8 86 91.3 91 Vicat Softening Point, ° C. 54 57 60.5 60 56 69 Tensile @ Break, MPa 33.9 33.5 24.1 23.6 32.4 24 Elongation @ Break, % 403 421 472 427 473 520 Hardness, Shore D 58 58 51 50 56 52 Flexural Modulus, MPa 289 290 152 141 282 150

It has been determined that when hard/soft ionomer blends are used for the outer cover layer, good results are achieved when the relative combination is in a range of about 3–25 percent hard ionomer and about 75–97 percent soft ionomer.

Moreover, in alternative embodiments, the inner and/or outer cover layer formulation may also comprise up to 100 wt % of a non-ionomeric thermoplastic or thermoset material including a thermoplastic polyester polyurethane such as B.F. Goodrich Company's Estane® polyester polyurethane X-4517 or a reaction-injection molded material such as one or more of the Bayflex RIM polyurethanes from Bayer. The non-ionomeric thermoplastic material may be blended with a soft ionomer. For example, polyamides blend well with soft ionomer. The properties for Estane® X-4517 were previously noted.

Other soft, relatively low modulus non-ionomeric thermoplastic or thermoset materials may also be utilized to produce the inner and/or outer cover layer as long as the non-ionomeric materials produce the playability and durability characteristics desired without adversely effecting the enhanced travel distance characteristic produced by the high acid ionomer resin composition. These include, but are not limited to thermoplastic polyurethanes such as Texin thermoplastic polyurethanes from Mobay Chemical Co. and the Pellethane thermoplastic polyurethanes from Dow Chemical Co.; non-ionomeric thermoset polyurethanes including but not limited to those disclosed in U.S. Pat. No. 5,334,673; cross-linked metallocene catalyzed polyolefins; ionomer/rubber blends such as those in Spalding U.S. Pat. Nos. 4,986,545; 5,098,105 and 5,187,013; and, styrene-butadiene-styrene block copolymers, including functionalized styrene-butadiene-styrene block copolymers, styrene-ethylene-butadiene-styrene (SEBS) block copolymers such as KRATON materials from Shell Chemical Co., including functionalized SEBS block copolymers; and, Hytrel polyester elastomers from DuPont and Pebax polyesteramides from Elf Atochem S.A.

Notwithstanding the foregoing, it is most preferred to utilize a reaction injection molded (RIM) polyurethane cover as described herein.

The preferred method of forming a cover for a golf ball according to the invention is by reaction injection molding (RIM). This process was previously described in conjunction with forming a mantle or inner cover layer.

The most preferred commercially available polyurethane material for forming golf ball covers in accordance with the present invention is Bayflex MP-10,000 system from Bayer Corporation of Pittsburgh, Pa. Although the Bayflex MP-10,000 two component polyurethane system is purported to be proprietary, the following information is available, previously set forth in Tables 7 and 8.

Additional non-limiting examples of suitable RIM systems for use in the present invention are Bayflex® elastomeric polyurethane RIM systems, Baydur® GS solid polyurethane RIM systems, Prism® solid polyurethane RIM systems, all from Bayer Corp. (Pittsburgh, Pa.), SPECTRIM reaction moldable polyurethane and polyurea systems from Dow Chemical USA (Midland, Mich.), including SPECTRIM MM 373-A (isocyanate) and 373-B (polyol), and Elastolit SR systems from BASF (Parsippany, N.J.). Preferred RIM systems include Bayflex® MP-10,000 and Bayflex® 110–50, filled and unfilled. Further preferred examples are polyols, polyamines and isocyanates formed by processes for recycling polyurethanes and polyureas.

Core

The cores of the inventive golf balls typically have a coefficient of restitution of about 0.750 or more, more preferably 0.770 or more and a PGA compression of about 90 or less, and more preferably 70 or less. The core used in the golf ball of the invention preferably is solid and can be wound or liquid filled. The term “solid cores” as used herein refers not only to one piece cores but also to those cores having a separate solid layer beneath the covers and over the central core. The cores have a weight of 25–40 grams and preferably 30–40 grams. When the golf ball of the invention has a solid core, this core can be compression molded from a slug of uncured or lightly cured elastomer composition comprising a high cis content polybutadiene and a metal salt of an α, β, ethylenically unsaturated carboxylic acid such as zinc mono- or diacrylate or methacrylate. To achieve higher coefficients of restitution and/or to increase hardness in the core, the manufacturer may include a small amount of a metal oxide such as zinc oxide. In addition, larger amounts of metal oxide than are needed to achieve the desired coefficient may be included in order to increase the core weight so that the finished ball more closely approaches the U.S.G.A. upper weight limit of 1.620 ounces. Non-limiting examples of other materials which may be used in the core composition including compatible rubbers or ionomers, and low molecular weight fatty acids such as stearic acid. Free radical initiator catalysts such as peroxides are admixed with the core composition so that on the application of heat and pressure, a curing or cross-linking reaction takes place.

As indicated above, a thread wound core may comprise a liquid, solid, gel or multi-piece center. The thread wound core is typically obtained by winding a thread of natural or synthetic rubber, or thermoplastic or thermosetting elastomer such as polyurethane, polyester, polyamide, etc. on a solid, liquid, gel or gas filled center to form a thread rubber layer that is then covered with one or more mantle or cover layers. Additionally, prior to applying the cover layers, the thread wound core may be further treated or coated with an adhesive layer, protective layer, or any substance that may improve the integrity of the wound core during application of the cover layers and ultimately in usage as a golf ball. Since the core material is not an integral part of the present invention, further detailed discussion concerning the specific types of core materials which may be utilized with the cover compositions of the invention are not specifically set forth herein.

Golf ball cores also can be made using the materials and processes described herein. To make a golf ball core using RIM polyurethane, the same processing conditions are used as are described herein with respect to covers. One difference is, of course, that no retractor pins are needed in the mold. Furthermore, an undimpled, smaller mold is used. If, however, a one piece ball is desired, a dimpled mold would be used. Polyurethanes also can be used for cores.

Method of Making Golf Ball

In preparing golf balls in accordance with the present invention, a mantle layer or inner cover layer is molded (both by injection molding or by compression molding) about a core (preferably a solid core). A comparatively softer outer layer is molded over the mantle or inner cover layer.

The solid core for the multi-layer ball is about 1.2–1.6 inches in diameter, although it may be possible to use cores in the range of about 1.0–2.0 inches. Conventional solid cores are typically compression or injection molded from a slug or ribbon of uncured or lightly cured elastomer composition comprising a high cis content polybutadiene and metal salt of an α, β, ethylenically unsaturated carboxylic acid such as zinc mono or diacrylate or methacrylate. To achieve higher coefficients of restitution in the core, the manufacturer may include fillers such as small amounts of a metal oxide such as zinc oxide. In addition, larger amounts of metal oxide than those that are needed to achieve the desired coefficient are often included in conventional cores in order to increase the core weight so that the finished ball more closely approaches the U.S.G.A. upper weight limit of 1.620 ounces. Other materials may be used in the core composition including compatible rubbers or ionomers, and low molecular weight fatty acids such as stearic acid. Free radical initiators such as peroxides are admixed with the core composition so that on the application of heat and pressure, a complex curing cross-linking reaction takes place.

The mantle or inner cover layer which is molded over core is about 0.01 inches to about 0.10 inches in thickness, preferably about 0.03–0.07 inches thick. The inner ball which includes the core, one or more mantle or inner cover layers preferably has a diameter in the range of 1.25 to 1.60 inches. The outer cover layer is about 0.01 inches to about 0.10 inches in thickness. Together, the core, the optional mantle, and/or inner cover layers and the outer cover layer combine to form a ball having a diameter of 1.680 inches or more, the minimum diameter permitted by the rules of the United States Golf Association and weighing no more than 1.62 ounces.

In a particularly preferred embodiment of the invention, the golf ball has a dimple pattern which provides coverage of 65% or more. The golf ball typically is coated with a durable, abrasion-resistant, relatively non-yellowing finish coat.

The golf balls of the present invention can be produced by molding processes which include but are not limited to those which are currently well known in the golf ball art. For example, the golf balls can be produced by injection molding or compression molding the novel cover and/or mantle compositions around a wound or solid molded core to produce an inner ball which typically has a diameter of about 1.50 to 1.67 inches. The outer layer is subsequently molded over the inner layer to produce a golf ball having a diameter of 1.620 inches or more, preferably about 1.680 inches or more. Although either solid cores or wound cores can be used in the present invention, as a result of their lower cost and superior performance, solid molded is cores are preferred over wound cores. The standards for both the minimum diameter and maximum weight of the balls are established by the United States Golf Association (U.S.G.A.).

In compression molding, the inner cover composition is formed via injection at about 380° F. to about 450° F. into smooth surfaced hemispherical shells which are then positioned around the core in a mold having the desired inner cover thickness and subjected to compression molding at 2000 to 300° F. for about 2 to 10 minutes, followed by cooling at 500 to 70° F. for about 2 to 7 minutes to fuse the shells together to form a unitary intermediate ball. In addition, the intermediate balls may be produced by injection molding wherein the inner cover layer is injected directly around the core placed at the center of an intermediate ball mold for a period of time in a mold temperature of from 50° to about 100° F. Subsequently, the outer cover layer is molded around the core and the inner layer by similar compression or injection molding techniques to form a dimpled golf ball of a diameter of 1.680 inches or more.

Referring to FIG. 3, a process flow diagram for forming a RIM cover or mantle of polyurethane is shown. Isocyanate from bulk storage is fed through line 80 to an isocyanate tank 100. The isocyanate is heated to the desired temperature, e.g. 90 to about 150° F., by circulating it through heat exchanger 82 via lines 84 and 86. Polyol, polyamine, or another compound with an active hydrogen atom is conveyed from bulk storage to a polyol tank 108 via line 88. The polyol is heated to the desired temperature, e.g. 90 to about 150° F., by circulating it through heat exchanger 90 via lines 92 and 94. Dry nitrogen gas is fed from nitrogen tank 96 to isocyanate tank 100 via line 97 and to polyol tank 108 via line 98. Isocyanate is fed from isocyanate tank 100 via line 102 through a metering cylinder or metering pump 104 into recirculation mix head inlet line 106. Polyol is fed from polyol tank 108 via line 110 through a metering cylinder or metering pump 112 into a recirculation mix head inlet line 114. The recirculation mix head 116 receives isocyanate and polyol, mixes them, and provides for them to be fed through nozzle 118 into injection mold 120. The injection mold 120 has a top mold 122 and a bottom mold 124. Mold heating or cooling can be performed through lines 126 in the top mold 122 and lines 140 in the bottom mold 124. The materials are kept under controlled temperature conditions to insure that the desired reaction profile is maintained.

The polyol component typically contains additives, such as stabilizers, flow modifiers, catalysts, combustion modifiers, blowing agents, fillers, pigments, optical brighteners, and release agents to modify physical characteristics of the cover. Recycled polyurethane/polyurea also can be added to the core. Polyurethane/polyurea constituent molecules that were derived from recycled polyurethane can be added in the polyol component.

Inside the mix head 116, injector nozzles impinge the isocyanate and polyol at ultra-high velocity to provide excellent mixing. Additional mixing preferably is conducted using an aftermixer 130, which typically is constructed inside the mold between the mix head and the mold cavity.

As is shown in FIG. 4, the mold includes a golf ball cavity chamber 132 in which a spherical golf ball cavity 134 with a dimpled, inner spherical surface 136 is defined. The aftermixer 130 can be a peanut aftermixer, as is shown in FIG. 3, or in some cases another suitable type, such as a heart, harp or dipper. However, the aftermixer does not have to be incorporated into the mold design. An overflow channel 138 receives overflow material from the golf ball cavity 134 through a shallow vent 142. Heating/cooling passages 126 and 140, which preferably are in a parallel flow arrangement, carry heat transfer fluids such as water, oil, etc. through the top mold 122 and the bottom mold 124. It will be appreciated that in forming a mantle via this technique, the mold need not provide a dimpled surface.

The mold cavity contains retractable pins and is generally constructed in the same manner as a mold cavity used to injection mold a thermoplastic, e.g., ionomeric golf ball cover. However, two differences when RIM is used are that tighter pin tolerances generally are required, and a lower injection pressure is used. Also, the molds can be produced from lower strength material such as aluminum.

The golf balls formed according to the present invention can be coated using a conventional two-component spray coating or can be coated during the RIM process, i.e., using an in-mold coating process.

After molding, the golf balls produced may undergo various further processing steps such as buffing, painting and marking as disclosed in U.S. Pat. No. 4,911,451.

The RIM process used in forming components of a multi-layered golf ball disclosed herein is substantially different from, and advantageous over, the conventional injection and compression molding techniques.

First, during the RIM process of the present application, the chemical reaction, i.e., the mixture of isocyanate from the isocyanate tank and polyol from the polyol tank, occurs during the molding process. Specifically, the mixing of the reactants occurs in the recirculation mix head and the after mixer, both of which are connected directly to the injection mold. The reactants are simultaneously mixed and injected into the mold, forming the desired component.

Typically, prior art techniques utilize mixing of reactants to occur before the molding process. Mixing under either compression or injection molding occurs in a mixer that is not connected to the molding apparatus. Thus, the reactants must first be mixed in a mixer separate from the molding apparatus, then added into the apparatus. Such a process causes the mixed reactants to first solidify, then later melt in order to properly mold.

Second, the RIM process requires lower temperatures and pressures during molding than does injection or compression molding. Under the RIM process, the molding temperature is maintained at about 100–120° F. in order to ensure proper injection viscosity. Compression molding is typically completed at a higher molding temperature of about 320° F. (160° C.). Injection molding is completed at even a higher temperature range of 392–482° F. (200–250° C.). Molding at a lower temperature is beneficial when, for example, the cover is molded over a very soft core so that the very soft core does not melt or decompose during the molding process.

Third, the RIM process creates more favorable durability properties in a golf ball than does conventional injection or compression molding. The preferred process of the present invention provides improved durability for a golf ball cover or mantle by providing a uniform or “seamless” cover in which the properties of the cover material in the region along the parting line are generally the same as the properties of the cover material at other locations on the cover, including at the poles. The improvement in durability is due to the fact that the reaction mixture is distributed uniformly into a closed mold. This uniform distribution of the injected materials eliminates knit-lines and other molding deficiencies which can be caused by temperature difference and/or reaction difference in the injected materials. The RIM process of the present invention results in generally uniform molecular structure, density and stress distribution as compared to conventional injection molding processes, where failure along the parting line or seam of the mold can occur because the interfacial region is intrinsically different from the remainder of the cover layer or mantle and, thus, can be weaker or more stressed.

Fourth, the RIM process is relatively faster than the conventional injection and compression molding techniques. In the RIM process, the chemical reaction takes place in under 5 minutes, typically in less than two minutes, preferably in under one minute and, in many cases, in about 30 seconds or less. The demolding time of the present application is 10 minutes or less. The molding process alone for the conventional methods typically take about 15 minutes. Thus, the overall speed of the RIM process makes it advantageous over the injection and compression molding methods.

The resulting golf ball produced from the hard inner layer and the relatively softer, low flexural modulus outer layer provide for an improved multilayer golf ball which provides for desirable coefficient of restitution and durability properties while at the same time offering the feel and spin characteristics associated with soft balata and balata-like covers of the prior art.

Unique Spin Characteristics

As indicated above, the golf ball of the invention is unique in that it provides good distance when hit with a driver, good control off of irons, and excellent spin on short chip shots. This golf ball is superior to conventional soft covered two-piece or wound balls in that it has lower spin off of a driver and higher spin on short shots.

The spin factor of the ball of the invention may be specified in the manner described below.

Step 1. A golf ball testing machine is set up in order that it meets the following conditions for hitting a 1995 Top-Flite Tour Z-balata 90 ball produced by Spalding & Evenflo Companies.

Club Launch Angle Ball Speed Spin Rate 9 iron 21 ± 1.5 160.5 ± 9.0 9925 ± 600 The machine is set up such that the above conditions are met for each test using 10 Z-balata 90 golf balls which are hit 3 times each at the same machine setting. The thirty measurements of spin rate are averaged to obtain N_(91-ZB).

Step 2. Ten golf balls of the invention (Ball X) are hit 3 times each using the same machine setting as was used for the Z-balata balls and spin date is collected. Any clearly erratic spin test result is eliminated and replaced by a new test with the same ball. The thirty measurements of spin rate are averaged to obtain N_(91-X).

Step 3. The machine is set up in order that it meets the following conditions for hitting a 1995 Z-balata 90 ball, the conditions being intended to replicate a 30-yard chip shot:

Club Launch Angle Ball Speed Spin Rate Sand Wedge 28 ± 4.5 58.0 ± 4.0 4830 ± 770 The machine is set up such that the above conditions are met for each test using 10 Z-balata 90 golf balls which are hit 3 times each at the same machine setting. The thirty measurements of spin rate are averaged to obtain N_(SW-ZB).

Step 4. The 10 golf balls used in Step 2 are hit three times each using the same machine setting as was used in Step 3 and spin data is collected. Any clearly erratic spin test result is eliminated and replaced by a new test with the same ball. The thirty measurements of spin rate are averaged to obtain N_(SW-X).

Step 5. The numerical values of N_(91-ZB), N_(91-X), N_(SW-ZB), N_(SW-X) are inserted into the following formula to obtain a spin factor:

${{Spin}\mspace{14mu}{factor}} = {\frac{N_{{SW}\text{-}X}}{N_{91\text{-}X}} - {\frac{N_{{SW}\text{-}{ZB}}}{N_{91\text{-}{ZB}}} \times 100}}$

The golf ball of the invention has a spin factor of 3.0 or more, more preferably 5.0 or more, and most preferably 8.0 or more.

Definitions

Coefficient of Restitution

As is apparent from the above discussions, two principal properties involved in golf ball performance are resilience and PGA compression. The resilience or coefficient of restitution (COR) of a golf ball is the constant “e,” which is the ratio of the relative velocity of an elastic sphere after direct impact to that before impact. As a result, the COR (“e”) can vary from 0 to 1, with 1 being equivalent to a perfectly or completely elastic collision and 0 being equivalent to a perfectly or completely inelastic collision.

COR, along with additional factors such as club head speed, club head mass, ball weight, ball size and density, spin rate, angle of trajectory and surface configuration (i.e., dimple pattern and area of dimple coverage) as well as environmental conditions (e.g. temperature, moisture, atmospheric pressure, wind, etc.) generally determine the distance a ball will travel when hit. Along this line, the distance a golf ball will travel under controlled environmental conditions is a function of the speed and mass of the club and size, density and resilience (COR) of the ball and other factors. The initial velocity of the club, the mass of the club and the angle of the ball's departure are essentially provided by the golfer upon striking. Since club head, club head mass, the angle of trajectory and environmental conditions are not determinants controllable by golf ball producers and the ball size and weight are set by the U.S.G.A., these are not factors of concern among golf ball manufacturers. The factors of determinants of interest with respect to improved distance are generally the coefficient of restitution (COR) and the surface configuration (dimple pattern, ratio of land area to dimple area, etc.) of the ball.

The COR of solid core balls is a function of the composition of the core and of the cover. The core and/or cover may be comprised of one or more layers such as in multi-layered balls. In balls containing a wound core (i.e., balls comprising a liquid or solid center, elastic windings, and a cover), the coefficient of restitution is a function of not only the composition of the center and cover, but also the composition and tension of the elastomeric windings. As in the solid core balls, the center and cover of a wound core ball may also consist of one or more layers. The COR of the golf balls of the present invention is a function of the composition and physical properties of the core and cover layer materials such as flex modulus, hardness and particularly, their resilience, i.e. ability to quickly recover from a high impact deformation.

The coefficient of restitution is the ratio of the outgoing velocity to the incoming velocity. In the examples of this application, the coefficient of restitution of a golf ball was measured by propelling a ball horizontally at a speed of 125±5 feet per second (fps) and corrected to 125 fps against a generally vertical, hard, flat steel plate and measuring the ball's incoming and outgoing velocity electronically. Speeds were measured with a pair of Oehler Mark 55 ballistic screens available from Oehler Research, Inc., P.O. Box 9135, Austin, Tex. 78766, which provide a timing pulse when an object passes through them. The screens were separated by 36″ and are located 25.25″ and 61.25″ from the rebound wall. The ball speed was measured by timing the pulses from screen 1 to screen 2 on the way into the rebound wall (as the average speed of the ball over 36″), and then the exit speed was timed from screen 2 to screen 1 over the same distance. The rebound wall was tilted 2 degrees from a vertical plane to allow the ball to rebound slightly downward in order to miss the edge of the cannon that fired it. The rebound wall is solid steel 2.0 inches thick.

As indicated above, the incoming speed should be 125±5 fps but corrected to 125 fps. The correlation between COR and forward or incoming speed has been studied and a correction has been made over the ±5 fps range so that the COR is reported as if the ball had an incoming speed of exactly 125.0 fps.

The coefficient of restitution must be carefully controlled in all commercial golf balls if the ball is to be within the specifications regulated by the United States Golf Association (U.S.G.A.). As mentioned to some degree above, the U.S.G.A. standards indicate that a “regulation” ball cannot have an initial velocity exceeding 255 feet per second in an atmosphere of 75° F. when tested on a U.S.G.A. machine. Since the coefficient of restitution of a ball is related to the ball's initial velocity, it is highly desirable to produce a ball having sufficiently high coefficient of restitution to closely approach the U.S.G.A. limit on initial velocity, while having an ample degree of softness (i.e. hardness) to produce enhanced playability (i.e., spin, etc).

PGA Compression

PGA compression is another important property involved in the performance of a golf ball. The compression of the ball can affect the playability of the ball on striking and the sound or “click” produced. Similarly, compression can affect the “feel” of the ball (i.e., hard or soft responsive feel), particularly in chipping and putting.

Moreover, while compression itself has little bearing on the distance performance of a ball, compression can affect the playability of the ball on striking. The degree of compression of a ball against the club face and the softness of the cover strongly influences the resultant spin rate. Typically, a softer cover will produce a higher spin rate than a harder cover. Additionally, a harder core will produce a higher spin rate than a softer core. This is because at impact a hard core serves to compress the cover of the ball against the face of the club to a much greater degree than a soft core thereby resulting in more “grab” of the ball on the clubface and subsequent higher spin rates. In effect the cover is squeezed between the relatively incompressible core and clubhead. When a softer core is used, the cover is under much less compressive stress than when a harder core is used and therefore does not contact the clubface as intimately. This results in lower spin rates. The term “compression” utilized in the golf ball trade generally defines the overall deflection that a golf ball undergoes when subjected to a compressive load. For example, PGA compression indicates the amount of change in golf ball's shape upon striking.

In the past, PGA compression related to a scale of from 0 to 200 given to a golf ball. The lower the PGA compression value, the softer the feel of the ball upon striking. In practice, tournament quality balls have compression ratings around 70–100, preferably around 80 to 100.

In determining PGA compression using the 0–200 scale, a standard force is applied to the external surface of the ball. A ball which exhibits no deflection (0.0 inches in deflection) is rated 200 and a ball which deflects 2/10th of an inch (0.2 inches) is rated 0. Every change of 0.001 of an inch in deflection represents a 1 point drop in compression. Consequently, a ball which deflects 0.1 inches (100×0.001 inches) has a PGA compression value of 100 (i.e., 200–100) and a ball which deflects 0.100 inches (110×0.001 inches) has a PGA compression of 90 (i.e., 200–110).

In order to assist in the determination of compression, several devices have been employed by the industry. For example, PGA compression is determined by an apparatus fashioned in the form of a small press with an upper and lower anvil. The upper anvil is at rest against a 200-pound die spring, and the lower anvil is movable through 0.300 inches by means of a crank mechanism. In its open position the gap between the anvils is 1.780 inches allowing a clearance of 0.100 inches for insertion of the ball. As the lower anvil is raised by the crank, it compresses the ball against the upper anvil, such compression occurring during the last 0.200 inches of stroke of the lower anvil, the ball then loading the upper anvil which in turn loads the spring. The equilibrium point of the upper anvil is measured by a dial micrometer if the anvil is measured by a dial micrometer if the anvil is deflected by the ball more than 0.100 inches (less deflection is simply regarded as zero compression) and the reading on the micrometer dial is referred to as the compression of the ball. In practice, tournament quality balls have compression ratings around 80 to 100 which means that the upper anvil was deflected a total of 0.120 to 0.100 inches.

An example to determine PGA compression can be shown by utilizing a golf ball compression tester produced by Atti Engineering Corporation of Newark, N.J. The value obtained by this tester relates to an arbitrary value expressed by a number which may range from 0 to 100, although a value of 200 can be measured as indicated by two revolutions of the dial indicator on the apparatus. The value obtained defines the deflection that a golf ball undergoes when subjected to compressive loading. The Atti test apparatus consists of a lower movable platform and an upper movable spring-loaded anvil. The dial indicator is mounted such that it measures the upward movement of the springloaded anvil. The golf ball to be tested is placed in the lower platform, which is then raised a fixed distance. The upper portion of the golf ball comes in contact with and exerts a pressure on the springloaded anvil. Depending upon the distance of the golf ball to be compressed, the upper anvil is forced upward against the spring.

Alternative devices have also been employed to determine compression. For example, Applicant also utilizes a modified Riehle Compression Machine originally produced by Riehle Bros. Testing Machine Company, Phil., Pa. to evaluate compression of the various components (i.e., cores, mantle cover balls, finished balls, etc.) of the golf balls. The Riehle compression device determines deformation in thousandths of an inch under a load designed to emulate the 200 pound spring constant of the Atti or PGA compression testers. Using such a device, a Riehle compression of 61 corresponds to a deflection under load of 0.061 inches.

Additionally, an approximate relationship between Riehle compression and PGA compression exists for balls of the same size. It has been determined by Applicant that Riehle compression corresponds to PGA compression by the general formula PGA compression=160−Riehle compression. Consequently, 80 Riehle compression corresponds to 80 PGA compression, 70 Riehle compression corresponds to 90 PGA compression, and 60 Riehle compression corresponds to 100 PGA compression. For reporting purposes, Applicant's compression values are usually measured as Riehle compression and converted to PGA compression.

Furthermore, additional compression devices may also be utilized to monitor golf ball compression so long as the correlation to PGA compression is known. These devices have been designed, such as a Whitney Tester, to correlate or correspond to PGA compression through a set relationship or formula.

Shore D Hardness

As used herein, “Shore D hardness” of a cover is measured generally in accordance with ASTM D-2240, except the measurements are made on the curved surface of a molded cover, rather than on a plaque. Furthermore, the Shore D hardness of the cover is measured while the cover remains over the core. When a hardness measurement is made on a dimpled cover, Shore D hardness is measured at a land area of the dimpled cover.

Fillers

In a particularly preferred form of the invention, at least one layer of the golf ball contains at least 0.01 parts by weight of a filler. Fillers preferably are used to adjust the density, flex modulus, mold release, and/or melt flow index of a layer. More preferably, at least when the filler is for adjustment of density or flex modulus of a layer, it is present in an amount of at least five parts by weight based upon 100 parts by weight of the layer composition. With some fillers, up to about 200 parts by weight probably can be used.

A density adjusting filler according to the invention preferably is a filler which has a specific gravity which is at least 0.05 and more preferably at least 0.1 higher or lower than the specific gravity of the layer composition. Particularly preferred density adjusting fillers have specific gravities which are higher than the specific gravity of the resin composition by 0.2 or more, even more preferably by 2.0 or more.

A flex modulus adjusting filler according to the invention is a filler which, when used in amount of e.g. 1–100 parts by weight based upon 100 parts by weight of resin composition, will raise or lower the flex modulus (ASTM D-790) of the resin composition by at least 1% and preferably at least 5% as compared to the flex modulus of the resin composition without the inclusion of the flex modulus adjusting filler.

A mold release adjusting filler is a filler which allows for the easier removal of a part from a mold, and eliminates or reduces the need for external release agents which otherwise could be applied to the mold. A mold release adjusting filler typically is used in an amount of up to about 2 wt % based upon the total weight of the layer.

A melt flow index adjusting filler is a filler which increases or decreases the melt flow, or ease of processing of the composition.

The layers may contain coupling agents that increase adhesion of materials within a particular layer e.g. to couple a filler to a resin composition, or between adjacent layers. Non-limiting examples of coupling agents include titanates, zirconates and silanes. Coupling agents typically are used in amounts of 0.1–2 wt % based upon the total weight of the composition in which the coupling agent is included.

A density adjusting filler is used to control the moment of inertia, and thus the initial spin rate of the ball and spin decay. The addition in one or more layers, and particularly in the outer cover layer of a filler with a lower specific gravity than the resin composition results in a decrease in moment of inertia and a higher initial spin rate than would result if no filler were used. The addition in one or more of the cover layers, and particularly in the outer cover layer of a filler with a higher specific gravity than the resin composition, results in an increase in moment of inertia and a lower initial spin rate. High specific gravity fillers are preferred as less volume is used to achieve the desired inner cover total weight. Nonreinforcing fillers are also preferred as they have minimal effect on COR. Preferably, the filler does not chemically react with the resin composition to a substantial degree, although some reaction may occur when, for example, zinc oxide is used in a shell layer which contains some ionomer.

The density-increasing fillers for use in the invention preferably have a specific gravity in the range of 1.0–20. The density-reducing fillers for use in the invention preferably have a specific gravity of 0.06–1.4, and more preferably 0.06–0.90. The flex modulus increasing fillers have a reinforcing or stiffening effect due to their morphology, their interaction with the resin, or their inherent physical properties. The flex modulus reducing fillers have an opposite effect due to their relatively flexible properties compared to the matrix resin. The melt flow index increasing fillers have a flow enhancing effect due to their relatively high melt flow versus the matrix. The melt flow index decreasing fillers have an opposite effect due to their relatively low melt flow index versus the matrix.

Fillers which may be employed in layers other than the outer cover layer may be or are typically in a finely divided form, for example, in a size generally less than about 20 mesh, preferably less than about 100 mesh U.S. standard size, except for fibers and flock, which are generally elongated. Flock and fiber sizes should be small enough to facilitate processing. Filler particle size will depend upon desired effect, cost, ease of addition, and dusting considerations. The filler preferably is selected from the group consisting of precipitated hydrated silica, clay, talc, asbestos, glass fibers, aramid fibers, mica, calcium metasilicate, barium sulfate, zinc sulfide, lithopone, silicates, silicon carbide, diatomaceous earth, polyvinyl chloride, carbonates, metals, metal alloys, tungsten carbide, metal oxides, metal stearates, particulate carbonaceous materials, micro balloons, and combinations thereof. Non-limiting examples of suitable fillers, their densities, and their preferred uses are as follows in Table 15:

TABLE 15 Filler Type Specific Gravity Comments Precipitated hydrated silica 2.0 1, 2 Clay 2.62 1, 2 Talc 2.85 1, 2 Asbestos 2.5 1, 2 Glass fibers 2.55 1, 2 Aramid fibers (KEVLAR ®) 1.44 1, 2 Mica 2.8 1, 2 Calcium metasilicate 2.9 1, 2 Barium sulfate 4.6 1, 2 Zinc sulfate 4.1 1, 2 Lithopone 4.2–4.3 1, 2 Silicates 2.1 1, 2 Silicon carbide platelets 3.18 1, 2 Silicon carbide whiskers 3.2 1, 2 Tungsten carbide 15.6 1   Diatomaceous earth 2.3 1, 2 Polyvinyl chloride 1.41 1, 2 Carbonates Calcium carbonate 2.71 1, 2 Magnesium carbonate 2.20 1, 2 Metals and Alloys (powders) Titanium 4.51 1   Tungsten 19.35 1   Aluminum 2.70 1   Bismuth 9.78 1   Nickel 8.90 1   Molybdenum 10.2 1   Iron 7.86 1   Steel 7.8–7.9 1   Lead 11.4 1, 2 Copper 8.94 1   Brass 8.2–8.4 1   Boron 2.34 1   Boron carbide whiskers 2.52 1, 2 Bronze 8.70–8.74 1   Cobalt 8.92 1   Beryllium 1.84 1   Zinc 7.14 1   Tin 7.31 1   Metal Oxides Zinc oxide 5.57 1, 2 Iron oxide 5.1 1, 2 Aluminum oxide 4.0 Titanium oxide 3.9–4.1 1, 2 Magnesium oxide 3.3–3.5 1, 2 Zirconium oxide 5.73 1, 2 Metal Stearates Zinc stearate 1.09 3, 4 Calcium stearate 1.03 3, 4 Barium stearate 1.23 3, 4 Lithium stearate 1.01 3, 4 Magnesium stearate 1.03 3, 4 Particulate carbonaceous materials Graphite 1.5–1.8 1, 2 Carbon black 1.8 1, 2 Natural bitumen 1.2–1.4 1, 2 Cotton flock 1.3–1.4 1, 2 Cellulose flock 1.15–1.5  1, 2 Leather fiber 1.2–1.4 1, 2 Micro balloons Glass 0.15–1.1  1, 2 Ceramic 0.2–0.7 1, 2 Fly ash 0.6–0.8 1, 2 Coupling Agents Adhesion Promotors Titanates 0.95–1.17 Zirconates 0.92–1.11 Silane 0.95–1.2  COMMENTS: 1 Particularly useful for adjusting density of the cover layer. 2 Particularly useful for adjusting flex modules of the cover layer. 3 Particularly useful for adjusting mold release of the cover layer. 4 Particularly useful for increasing melt flow index of the cover layer.

All fillers except for metal stearates would be expected to reduce the melt flow index of the cover layer.

The amount of filler employed is primarily a function of weight requirements and distribution.

The present invention is further illustrated by the following examples in which the parts of the specific ingredients are by weight. It is to be understood that the present invention is not limited to the examples, and various changes and modifications may be made in the invention without departing from the spirit and scope thereof.

EXAMPLE 1 Ionic Terpolymer-Containing Cover

A set of two-piece golf balls was made with solid cores and a cover composition of 75 weight % NUCREL 035, which is an acrylate ester-containing acid terpolymer, and 25 weight % of a masterbatch containing 4.5 weight % MgO Surlyn® 1605 (“MgO Masterbatch”). The terpolymer was reacted with the masterbatch at a temperature of about 250° F. under high shear conditions at a pressure of about 0 to 100 psi. The magnesium in the masterbatch neutralized acid groups of the terpolymer at a level of about 62% neutralization. The molded balls were finished with polyurethane primer and top coats. The PGA compression, coefficient of restitution, Shore C hardness, scuff resistance, spin rate and cold crack of the golf balls were determined. The results are shown on Table 16 below.

To measure cold crack, the finished golf balls were stored at −10° F. for at least 24 hours and were then subjected to 5 blows in a coefficient machine at 165 ft/sec. The balls were allowed to return to room temperature and were then visually inspected for cover cracking. None of the golf balls experienced cracking.

Coefficient of restitution (C.O.R.) was measured by firing the resulting golf ball in an air cannon at a velocity of 125 feet per second against a steel plate which was positioned 12 feet from the muzzle of the cannon. The rebound velocity was then measured. The rebound velocity was divided by the forward velocity to give the coefficient of restitution. Shore hardness was determined in general accordance with ASTM Test 2240, but was measured on a non-dimpled area of the surface of the golf ball.

COMPARATIVE EXAMPLE 1 Ionic Copolymer Cover (Non-Terpolymer)

A set of 12 two-piece golf balls was made according to the same procedure as that of Example 1 with the exception that NUCREL 925, a non-acrylate ester-containing acid copolymer was substituted for NUCREL 035. The resulting golf ball cover was too hard, resulting in four breaks during cold crack testing. The results are shown on Table 16.

COMPARATIVE EXAMPLE 2 Ionomer Non-Ionic Terpolymer Blend

The procedure of Example 1 was repeated with the exception that the MgO Masterbatch was replaced by pure Surlyn® 1605. All of the golf ball covers broke during cold crack testing. The results are shown on Table 16.

COMPARATIVE EXAMPLE 3 Ionomer Non-Ionic Copolymer Blend

The procedure of Comparative Example 1 was repeated with the exception that the MgO masterbatch was replaced by pure Surlyn® 1605. The results are shown on Table 16. When subjected to cold crack testing, all of the golf ball covers broke.

As can be seen from the results of Example 1 and Comparative Examples 1–3, inferior golf balls are obtained when a hard, non-acrylate ester-containing copolymer is used instead of a softer, acrylate ester-containing terpolymer, and when either an acrylate ester-containing acid terpolymer or a non-acrylate ester-containing acid copolymer is not neutralized with metal ions.

TABLE 16 Experiment Cover PGA COR (× Shore C Cold No. Material Weight Comp 1000) Hardness Crack 1.1 75% Nucrel 035/ 45.2 104 .783 80 No breaks 25% MgO MB in Surlyn 1605 Comp. 1 75% Nucrel 925/ 45.1 111 .798 90 4 breaks 25% MgO MB in Surlyn 1605 Comp. 2 75% Nucrel 035/ 45.1 99 .774 70 All broker 25% Surlyn 1605 Comp. 3 75% Nucrel 925/ 45.2 106 .790 75 All broke 25% Surlyn 1605

EXAMPLE 2 Ionic Terpolymers

An acrylate ester-containing terpolymer sold as ESCOR ATX 325 (Exxon Chemical Co.) was 57% neutralized with lithium cations. The ionomeric material, which also contained titanium dioxide, brightener, etc. from a white masterbatch, was placed over a solid golf ball core and the golf ball was primed and top coated. The properties of the resulting golf ball are shown on Table 18. This procedure was repeated using different combinations of terpolymers with cations and cation blends at the degrees of neutralization which are shown on Table 18. In the cation blends, mole ratios were about 1:1:1. All of the ATX materials shown on Table 18 are ESCOR ATX materials available from Exxon Chemical Co. The Nucrel materials are available from DuPont Chemical Co. Primacor 3440 is available from Dow Chemical Co.

The spin rate of the golf ball was measured by striking the resulting golf balls with a pitching wedge or 9-iron wherein the club-head speed is about 80 feet per second and the ball was launched at an angle of 26 to 34 degrees with an initial velocity of 100–115 feet per second. The spin rate was measured by observing the rotation of the ball in flight using stop action Strobe photography or via the use of a high speed video system.

The scuff resistance test was conducted in the following manner a Top-Flite tour pitching wedge (1994) with box grooves was obtained and was mounted in a Miyamae driving machine. The club face was oriented for a square hit. The forward/backward tee position was adjusted so that the tee was four inches behind the point in the downswing where the club was vertical. The height of the tee and toe-heel position of the club relative to the tee were adjusted in order that the center of the impact mark was about ¾ of an inch above the sole and was centered toe to heel across the face. The machine was operated at a club head speed of 125 feet per second. A minimum of three samples of each ball were tested. Each ball was hit three times:

After testing, the balls were rated according to the following Table 17:

TABLE 17 Rating Type of damage 1 Little or no damage (groove markings or dents) 2 Small cuts and/or ripples in cover 3 Moderate amount of material lifted from ball surface but still attached to ball 4 Material removed or barely attached The balls that were tested were primed and top coated.

As shown on Table 18, many of the cover materials resulted in golf balls having a scuff resistance of 1.50 less, and others had a scuff resistance rating of 1.5–25.

COMPARATIVE EXAMPLE 4 Hard/Soft Ionomer Blend

A golf ball with a cover formed from a blend of a commercially available hard sodium ionomer and a commercially available soft acrylate ester-containing zinc ionomer in which the blend contains less than 60 wt % soft ionomer was subjected to the same testing as the golf balls of Example 2. The results are shown on Table 18.

TABLE 18 Spin Rate Experiment Cover PGA COR (× Shore D Scuff (#9 Iron at No. Material Cation % Neuralization Comp. 1000) Hardness Resist. 105 ft/sec) Comp. 4 hard-soft Zn/Na 60% 90 787 58 4.0 9,859 ionomer blend 1 (control) 2-1  ATX 325 Li 57% 86 787 51 1.0 10,430 2-2  ATX 325 Li/Zn/K 65% 86 787 50 1.0 10,464 2-3  ATX 320 Li 57% N.T. N.T. 56 1.0 10,299 2-4  ATX 320 Li/Zn/K 65% 87 790 55 1.5 10,355 2-5  Nucrel Li — 89 803 65 3.0 7,644 010 2-6  Nucrel Li/Zn/K — 89 802 65 4.0 7,710 010 2-7  Nucrel Li — 87 801 62 3.0 8,931 035 2-8  Nucrel Li/Zn/K — 87 798 62 3.0 8,915 035 2-9  ATX 310 Li 53% 88 802 62 2.5 8,892 2-10 ATX 310 Li/Zn/K 60% 88 801 63 2.5 8,244 2-11 ATX 325 Li 57% 83 797 55 1.5 — 2-12 ATX 325 Li/Zn/K 65% 82 796 53 1.5 — 2-13 50% ATX (Li) 28.5%   89 777 50 1.5 — 325-Li 50% ATX 320-unneut. 2-14 75% ATX (Li/Zn/K) 49% 87 776 54 1.5 — 320-Li/Zn/K 25% ATX 320-unneut. 2-15 60% ATX (Li/Zn/K) 39% 88 779 54 1.5 — 325-Li/Zn/K 40% Primacor 3440-unneut. 2-16 ATX 320 Unneut. — 88 775 45 2.0 — 2-17 ATX 325 Unneut. — 88 — 42 1.5 — 2-18 ATX 325 Li 50% 95 797 50 1.0 — 2-19 ATX 325 Li 30% 96 791 46 1.5 — 2-20 ATX 325 Li/Zn/K 50% 91 791 48 1.0 — 2-21 ATX 325 Li/Zn/K 30% 90 N.T. 45 1.0 — 2-22 ATX 325 Li/Zn/K 50% 91 N.T. 47 1.0 —

EXAMPLE 3 Ionic Terpolymers

The procedure of Example 2 was repeated with the exception that single cations of lithium, magnesium, sodium and potassium were used in the cover material. The results are shown on Table 19.

As indicated on Table 19, the scuff resistance of the golf balls was 3.0 or better. The scuff resistance of the balls with covers made of an acrylic acid terpolymer was 1.0. For a given terpolymer, the scuff resistance did not change when different cations were used for neutralization.

TABLE 19 Experiment Cover % PGA COR (× Shore D Scuff No. Material Cation Neutralization Comp. 1000) Hardness Resistance 3-1 Nucrel 035 Li 100 90 792 62 3.0 3-2 Nucrel 035 Mg 100 89 792 62 3.0 3-3 ATX 325 Li 100 86 790 51 1.0 3-4 ATX 325 Mg 100 85 791 51 1.0 3-5 ATX 325 Na 81 85 790 51 1.0 3-6 ATX 325 K 95 85 791 51 1.0

COMPARATIVE EXAMPLE 5

Several intermediate balls (cores plus inner cover layers) were prepared in accordance with conventional molding procedures described above. The inner cover compositions were molded around 1.545 inch diameter cores weighing 36.5 grams with a specific gravity of about 1.17 such that the inner cover had a wall thickness of about 0.0675 inches and a specific gravity of about 0.95, with the overall ball measuring about 1.680 inches in diameter.

The cores utilized in the examples were comprised of the following ingredients: 100 parts by weight high cis-polybutadiene, 31 parts by weight zinc diacrylate, about 6 parts by weight zinc oxide, 20 parts by weight zinc stearate, 17–18 parts by weight calcium carbonate, and small quantities of peroxide, coloring agent and a polymeric isocyanate sold as Papi 94 (Dow Chemical Co.). The molded cores exhibited PGA compressions of about 100 and C.O.R. values of about 0.800.

The inner cover compositions designated herein as compositions A–E utilized to formulate the intermediate balls are set forth in Table 20 below. The resulting molded intermediate balls were tested to determine the individual compression (Riehle), C.O.R., Shore C hardness, spin rate and cut resistance properties. These results are also set forth in Table 20 below.

The data of these examples are the average of twelve intermediate balls produced for each example. The properties were measured according to the following parameters:

Cut resistance was measured in accordance with the following procedure: A golf ball was fired at 135 feet per second against the leading edge of a pitching wedge wherein the leading edge radius is 1/32 inch, the loft angle is 51 degrees, the sole radius is 2.5 inches and the bounce angle is 7 degrees.

The cut resistance of the balls tested herein was evaluated on a scale of 1 to 5. The number 1 represents a cut that extends completely through the cover to the core. A 2 represents a cut that does not extend completely through the cover but that does break the surface. A 3 does not break the surface of the cover but does leave a permanent dent. A 4 leaves only a slight crease which is permanent but not as severe as 3. A 5 represents virtually no visible indentation or damage of any sort.

The spin rate of the golf ball was measured by striking the resulting golf balls with a pitching wedge or 9 iron wherein the club head speed is about 105 feet per second and the ball is launched at an angle of 26 to 34 degrees with an initial velocity of about 110 to 115 feet per second. The spin rate was measured by observing the rotation of the ball in flight using stop action Strobe photography.

Initial velocity is the velocity of a ball when struck at a hammer speed of 143.8 feet per second in accordance with a test as prescribed by the U.S.G.A.

As will be noted, compositions A, B and C include high acid ionomeric resin's, with composition B further including zinc stearate. Composition D represents the inner layer (i.e. Surlyn® 1605) used in U.S. Pat. No. 4,431,193. Composition E provides a hard, low acid ionomeric resin.

The purpose behind producing and testing the balls of Table 20 was to provide a subsequent comparison in properties with the multi-layer golf balls of the present invention.

TABLE 20 Molded Intermediate Golf Balls A B C D E Ingredients of Inner Cover Com- positions Iotek 959 50 50 — — — Iotek 960 50 50 — — — Zinc Stearate — 50 — — — Surlyn 8162 — — 75 — — Surlyn 8422 — — 25 — — Surlyn 1605 — — — 100 — Iotek 7030 — — — — 50 Iotek 8000 — — — — 50 Properties of Molded Intermediate Balls Compression 58 58 60 63 62 C.O.R. .811 .810 .807 .793 .801 Shore C 98 98 97 96 96 Hardness Spin Rate 7,367 6,250 7,903 8,337 7,956 (R.P.M.) Cut 4–5 4–5 4–5 4–5 4–5 Resistance

As shown in Table 20 above, the high acid ionomer resin inner cover layer (molded intermediate balls A–c) have lower spin rates and exhibit substantially higher resiliency characteristics than the low acid ionomer resin based inner cover layers of balls D and E.

EXAMPLE 4

Multi-layer balls in accordance with the present invention were then prepared. Specifically, the inner cover compositions used to produce intermediate golf balls from Table 20 were molded over the solid cores to a thickness of about 0.0375 inches, thus forming the inner layer. The diameter of the solid core with the inner layer measured about 1.620 inches. Alternatively, the intermediate golf balls of Table 20 were ground down using a centerless grinding machine to a size of 1.620 inches in diameter to produce an inner cover layer of 0.0375 inches.

The size of 1.620 inches was determined after attempting to mold the outer cover layer to various sizes (1.600″, 1.610″, 1.620″, 1.630″ and 1.640″) of intermediate (core plus inner layer) balls. It was determined that 1.620″ was about the largest “intermediate” ball (i.e., core plus inner layer) which could be easily molded over with the soft outer layer materials of choice. The goal herein was to use as thin an outer layer as necessary to achieve the desired playability characteristics while minimizing the cost of the more expensive outer materials. However, with a larger diameter final golf ball and/or if the cover is compression molded, a thinner cover becomes feasible.

With the above in mind, an outer cover layer composition was blended together in accordance with conventional blending techniques. The outer layer composition used for this portion of the example is a relatively soft cover composition such as those listed in U.S. Pat. No. 5,120,791. An example of such a soft cover composition is a 45% soft/55% hard low acid ionomer blend designated by the inventor as “TE-90”. The composition of TE-90 is set forth as follows in Table 21

TABLE 21 Outer Cover Layer Composition TE-90 Iotek 8000 22.7 weight % Iotek 7030 22.7 weight % Iotek 7520 45.0 weight % White MB¹  9.6 weight % ¹White MB consists of about 23.77 weight percent TiO₂, 0.22 weight percent Uvitex O, 0.03 weight percent Santonox R₁ 0.05 weight percent Ultramarine blue and 75.85 weight percent Iotek 7030.

The above outer layer composition was molded around each of the 1.620 diameter intermediate balls comprising a core plus one of compositions A–D, respectively. In addition, for comparison purposes, Surlyn® 1855 (new Surlyn® 9020), the cover composition of the '193 patent, was molded about the inner layer of composition D (the intermediate ball representative of the '193 patent). The outer layer TE-90 was molded to a thickness of approximately 1.680 inches in diameter. The resulting balls (a dozen for each example) were tested and the various properties thereof are set forth in Table 22 as follows:

TABLE 22 Finished Balls 1 2 3 4 5 Ingredients: Inner Cover Composition A B C D D Outer Cover Composition TE-90 TE-90 TE-90 TE-90 Surlyn ® 9020 Properties of Molded Finished Balls: Compression   63   63   69   70   61 C.O.R.    .784    .778    .780    .770    .757 Shore C Hardness   88   88   88   88   89 Spin (R.P.M.) 8,825 8,854 8,814 8,990 8,846 Cut Resistance 3–4 3–4 3–4 3–4 1–2

As it will be noted in finished balls 1–4, by creating a multi-layer cover utilizing the high acid ionomer resins in the inner cover layer and the hard/soft low acid ionomer resin in the outer cover layer, higher compression and increased spin rates are noted over the single layer covers of Table 16. In addition, both the C.O.R. and the Shore C hardness are reduced over the respective single layer covers noted in the previous Tables. This was once agin particularly true with respect to the multi-layered balls containing the high acid ionomer resin in the inner layer (i.e. finished balls 1–5). In addition, with the exception of prior art ball 5 (i.e. the '193 patent), resistance to cutting remains good but is slightly decreased.

Furthermore, it is also noted that the use of the high acid ionomer resins as the inner cover material produces a substantial increase in the finished balls' overall distance properties. In this regard, the high acid ionomer resin inner covers of balls 1–3 produce an increase of approximately 10 points in C.O.R. over the low acid ionomer resin inner covers of balls 4 and about a 25 point increase over the prior art balls 5. Since an increase in 3 to 6 points in C.O.R. results in an average increase of about 1 yard in distance, such an improvement is deemed to be significant.

Several other outer layer formulations were prepared and tested by molding them around the core and inner cover layer combination to form balls each having a diameter of about 1.68 inches. First, B.F. Goodrich Estane®) X-4517 polyester polyurethane was molded about the core molded with inner layer cover formulation A. DuPont Surlyn® 9020 was molded about the core which was already molded with inner layer D. Similar properties tests were conducted on these golf balls and the results are set forth in Table 23 below:

TABLE 23 Finished Balls 6 7 Ingredients: Inner Cover Layer A D Composition Outer Cover Layer Estane ® Surlyn ® Composition 4517 9020 Properties of Molded Finished Balls: Compression 67 61 C.O.R. .774 .757 Shore C Hardness 74 89 Spin (R.P.M.) 10,061 8,846 Cut Resistance 3–4 1–2

The ball comprising inner layer formulation D and Surlyn® 9020 identifies the ball in the Nesbitt U.S. Pat. No. 4,431,193 patent. As is noted, the example provides for relatively high softness and spin rate though it suffers from poor cut resistance and low C.O.R. This ball is unacceptable by today's standards.

As for the Estane® X-4517 polyester polyurethane, a significant increase in spin rate over the TE-90 cover is noted along with an increase in spin rate over the TE-90 cover is noted along with an increased compression. However, the C.O.R. and Shore C values are reduced, while the cut resistance remains the same. Furthermore, both the Estane® X-4517 polyester polyurethane and the Surlyn® 9020 were relatively difficult to mold in such thin sections.

EXAMPLE 5

In order to analyze the change in characteristics produced by multi-layer golf balls (standard size) having inner cover layers comprised of ionomer resin blends of different acid levels, a series of experiments was run. A number of tests were performed, varying the type of core, inner cover layer and outer cover layer. The results are shown below on Table 24.

TABLE 24 Sample INNER OUTER THICK- COM # CORE LAYER THICKNESS COM/COR COVER NESS (Rhiele) COR SHORE D SPIN 8 1042 YELLOW NONE — SEE BELOW TOP 0.055″ 61 .800 68 7331 GRADE 9 1042 YELLOW NONE — SEE BELOW 959–60 0.055″ 56 .808 73 6516 10 SPECIAL 1.47″ 959/960 0.050″ 65/.805 959–960 0.055″ 48 .830 73 6258 11 1042 YELLOW NONE — SEE BELOW SD 90 0.055″ 62 .792 63 8421 12 SPECIAL 1.47″ TOP 0.050″ 66/.799 SD 90 0.055″ 55 .811 63 8265 GRADE 13 SPECIAL 1.47″ 959/960 0.050″ 65/.805 SD 90 0.055″ 53 .813 63 8254 14 SPECIAL 1.47″ TOP 0.050″ 66/.799 TOP 0.055″ 51 .819 68 7390 GRADE GRADE 15 1042 YELLOW NONE — SEE BELOW Z-BALATA 0.055″ 67 .782 55 9479 16 SPECIAL 1.47″ 959–960 0.050″ 65/.805 Z-BALATA 0.055″ 61 .800 55 9026 17 SPECIAL 1.47″ TOP 0.050″ 66/.799 Z-BALATA 0.055″ 60 .798 55 9262 GRADE 1042 YELLOW > COMP = 72, COR = .780 SPECIAL 1.47″ CORE > COMP = 67, COR = .782

In this regard, “Top Grade” or “TG” is a low acid inner cover ionomer resin blend comprising of 70.6% lotek 8000, 19.9% lotek 7010 and 9.6% white masterbatch. “959/960” is a 50/50 wt/wt blend of lotek 959/960. In this regard, Escor® or lotek 959 is a sodium ion neutralized ethylene-acrylic neutralized ethylene-acrylic acid copolymer. According to Exxon, loteks 959 and 960 contain from about 19.0 to about 21.0% by weight acrylic acid with approximately 30 to about 70 percent of the acid groups neutralized with sodium and zinc ions, respectively.

Furthermore, the low acid ionomer formulation for “SD 90” and “Z-Balata” are set forth below in Table 25:

TABLE 25 SD Cover ZB Cover 17.2% Surlyn 8320 19% Iotek 8000 7.5% Surlyn 8120 19% Iotek 7030 49% Surlyn 9910 52.5 Iotek 7520 16.4 Surlyn 8940 9.5% white MB 9.7% white MB

The data clearly indicates that higher C.O.R. and hence increase travel distance can be obtained by using multi-layered covered balls versus balls covered with single layers. However, some sacrifices in compression and spin are also noted. Further, as shown in comparing Example Nos. 12 vs. 13, Example Nos. 17 vs. 16, etc. use of lower acid level inner cover layers and relatively soft outer cover layers (i.e. 50 wt. % or more soft ionomer) produces softer compression and higher spin rates than the golf balls comprised of high acid inner cover layers. Consequently, use of blends of low acid ionomer resins to produce the inner layer of a multi-layer covered golf ball, produces not only enhanced travel distance but also enhanced compression and spin properties.

EXAMPLE 6

Multi-layer oversized golf balls were produced utilizing different ionomer resin blends as the inner cover layer (i.e., core plus inner cover layer is defined as “mantel”). The “ball data” of the oversized multi-layer golf balls in comparison with production samples of “Top-Flite® XL” and Top-Flite® Z-Balata” is set forth below in Table 26.

TABLE 26 21 Top- 22 Top- Flite ® Flite ® Z- 18 19 20 XL Balata 90 Core Data Size 1.43 1.43 1.43 1.545 1.545 COR .787 .787 .787 — — Mantel Data Material TG TG TG — — Size .161 1.61 1.61 — — Thickness .090 .090 .090 — — Shore D 68 68 68 — — Compression 57 57 57 — — COR .815 .815 .815 — — Ball Data Cover TG ZB SD TG ZB Size 1.725 1.723 1.726 1.681 1.683 Weight 45.2 45.1 45.2 45.3 45.5 Shore D 68 56 63 68 56 Compression 45 55 49 53 77 COR .820 .800 .810 .809 .797 Spin 7230 9268 8397 7133 9287

The results indicate that use of multi-layer covers enhances C.O.R. and travel distance. Further, the data shows that use of a blend of low 30 acid ionomer resins (.e., “Top Grade”) to form the inner cover layer in combination with a soft outer cover (ZB” or “SD”) produces enhanced spin and compression characteristics. The overall combination results in a relatively optimal golf ball with respect to characteristics of travel distance, spin and durability.

EXAMPLE 7

Golf balls 7-1, 7-2, 7-3 and 74 having the formulations shown on Table 27 were formed.

TABLE 27 Chemical Component 7-1 7-2 7-3 7-4 Core Data Size 1.47″ 1.47″ 1.47″ 1.47″ Weight 32.7 g 32.7 g 32.7 g 32.7 g PGA Compression 70 60 70 60 COR 780 770 780 770 Composition High cis polybutadiene 100 100 100 100 Zinc oxide 30.5 31.6 30.5 31.6 Core regrind 16 16 16 16 Zinc Stearate 16 16 16 16 Zinc Diacrytlate 22 20 22 20 Initiator 0.9 0.9 0.9 0.9 Inner Cover Layer Size 1.57″ 1.57′ 1.57″ 1.57′ Weight 38.4 g 38.4 g 38.4 g 38.4 g PGA Compression 83 75 83 75 COR 801 795 801 795 Thickness 0.050″ 0.050′ 0.050″ 0.050″ Hardness (Shore C/D) 97/70 97/70 97/70 97/70 Composition Iotek 1002   50%   50% 50% 50% Iotek 1003   50%   50% 50% 50% Outer Cover Layer Hardness (Shore CD) 71/46 71/46 71/46 71/46 Thickness 0.055″ 0.055″ 0.055″ 0.055″ Composition Iotek 7510 92.8% 92.8% 42% 42% Iotek 7520 42% 42% Iotek 7030  7.2%  7.2% 7.3%  7.3%  Lotek 8000 8.7%  8.7%  Whitener Package Unitane 0-110  2.3 phr  2.3 phr  2.3 phr  2.3 phr Eastobrite OB1 0.025 phr 0.025 phr 0.025 phr 0.025 phr Ultra Marine Blue 0.042 phr 0.042 phr 0.042 phr 0.042 phr Santanox R 0.004 phr 0.004 phr 0.004 phr 0.004 phr Final Ball Data Size 1.68″ 1.68″ 1.68″ 1.68″ Weight 45.4 g 45.4 g 45.4 g 45.4 g PGA Compression 85 78 85 78 COR 793 785 793 785

The balls of Example 7-2 were tested by a number of professional quality golfers using a driver, 5-iron, 9-iron, and sand wedge or pitching wedge. Each player used his own clubs and hit both the ball of Example 7-2 and a control ball, which was the 1995 two-piece Top-Flite Tour Z-balata 90. The Z-balata 90 has a 1.545″ core of about 36.8 g with a PGA compression of about 80 and a COR of about 0.794. The cover of the Z-balata 90 is about 0.068 in. thick, and is a blend of lotek 8000 and lotek 7510 with or without masterbatch containing lotek 7030. The cover with or without masterbatch containing lotek 7030. The cover has a Shore D hardness of about 55. The ball has a PGA compression of about 79 and a COR of about 0.788. Each player hit six of the balls of Example 7-2 and six Z-balata control balls one time each. For each shot, measurements were made of the initial launch conditions of the golf ball, including launch angle and ball speed. Furthermore, spin rates at initial launch, carry distance, and total distance were measured. The players hit full shots with the driver (1W), 5-iron (51) and 9-iron (91). With the sand wedge or pitching wedge (SW), the players hit about 30 yard chip shots. Data points were removed if determined to be “wild points.” A point was said to be wild if it fell outside 2 standard deviations of the 6-hit average. Initial launch conditions were determined using a highly accurate high speed stop action video photography system. The results are shown on Table 28.

As shown on Table 28, multi-layer ball 7-2 was longer than the Z-balata control when it with a 5-iron but only slightly longer than the Z-balata ball using a driver and 9-iron. The multi-layer ball 7-2 and the two-piece control were generally the same in overall distance using a driver. In each case, the multi-layer ball 7-2 had a higher spin rate off the 30-yard chip shot than the Z-balata. The spin rate of the ball of Example 7-2 was an average of 11.6% higher than the spin rate of the Z-balata control in the 30 yard chip shot.

TABLE 28 2-Piece Control 7-2 Multi-Layer Ball L.A. B.S. Spin Carry Total L.A. B.S. Spin Carry\ Total Player Club (Deg) (fps) (rpm) (yds) (yds) (Deg.) (Fps) (rpm) (yds) (yds)  1 1W 10.4 262.2 3537 272.5 288.9 10.0 262.3 3247 271.6 292.2  2 1W 9.5 240.1 3124 238.1 253.6 8.9 238.3 2935 236.3 257.4  3 1W 8.6 258.8 3695 254.1 259.9 6.3 251.2 3357 247.6 260.8  4 1W 10.9 252.6 2639 271.6 289.8 12.5 251.4 3066 279.0 296.7  5 1W 9.5 211.7 3627 237.2 255.2 9.4 208.7 3415 235.0 259.8  6 1W 10.2 242.0 3105 263.8 283.2 11.0 243.9 2903 267.6 288.4  7 1W 11.5 214.9 3089 265.4 279.0 11.6 212.6 3165 262.9 274.4  8 1W 9.7 239.5 3129 263.6 288.8 9.3 235.3 2884 257.2 276.8  9 1W 11.7 211.2 2939 231.4 255.8 11.3 208.5 2032 222.2 244.3 10 1W 10.2 244.0 2797 243.3 250.2 9.7 239.6 3072 236.8 251.1 11 1W 247.4 263.8 13.8 215.8 3916 245.4 268.8 AVE. 10.2 237.7 3168 253.5 269.8 10.3 233.4 3090 251.1 270.1  1 51 12.4 207.3 5942 198.3 209.8 11.8 206.3 5507 196.2 207.8  2 51 178.3 184.2 14.9 199.4 5094 182.2 187.8  3 51 10.9 196.8 6462 185.2 188.9 11.5 197.0 6009 187.4 193.4  4 51 14.4 205.5 6683 207.8 213.7 14.7 208.3 6601 207.5 217.8  5 51 13.6 183.3 6734 182.9 189.4 14.2 180.9 6380 184.2 190.7  6 51 12.4 204.5 5771 201.0 210.5 12.9 208.4 5414 208.0 218.3  7 51 14.1 184.3 6013 194.8 198.1 13.1 182.7 6000 192.9 200.0  8 51 12.8 187.2 6149 188.0 200.3 13.1 191.6 6183 191.7 202.0  9 51 13.2 176.5 6000 168.2 173.7 13.6 172.5 6166 169.7 174.3 10 51 13.9 199.9 7214 175.2 178.2 14.9 199.1 6237 169.0 170.2 11 51 14.2 179.5 6669 181.9 187.8 15.7 181.2 5338 184.0 190.7 AVE 13.2 192.5 6364 187.4 194.1 13.7 193.4 5903 188.4 195.7  1 91 20.0 168.1 9865 152.5 159.5 20.4 172.2 9210 153.4 159.6  2 91 21.8 165.9 9770 132.7 137.0 23.0 164.7 8949 132.7 134.6  3 91 19.9 154.3 10764 128.8 134.3 19.9 156.5 10161 129.8 135.0  4 91 22.7 166.4 10551 146.0 148.8 23.9 165.7 9990 150.3 154.2  5 91 22.1 147.4 9682 137.1 138.1 22.2 148.5 9324 139.3 141.7  6 91 19.4 169.7 8939 153.3 158.0 19.7 168.2 8588 156.2 163.5  7 91 20.4 151.1 9899 147.5 150.0 21.6 150.3 9084 148.6 151.3  8 91 18.5 143.0 9408 142.0 147.5 18.3 141.8 9038 141.2 144.8  9 91 20.0 134.5 9124 124.9 128.8 20.1 132.9 8834 125.0 128.9 10 91 23.2 156.1 10603 122.7 124.1 23.2 155.6 11017 116.2 116.3 11 91 21.5 149.4 9729 131.0 134.5 23.4 151.7 8686 133.3 136.8 AVE 20.9 155.1 9849 138.0 141.9 21.4 155.3 9353 138.7 142.4  1 SW 29.2 56.4 5647 24.8 58.9 6679  2 SW 26.6 57.4 5446 25.2 5787 5647  3 SW 25.8 64.1 4925 24.3 63.5 5550  4 SW 30.9 60.9 5837 31.1 57.9 6158  5 SW 20.3 56.7 4152 19.0 56.3 4288  6 SW 34.3 57.1 3798 32.4 61.5 4700  7 SW 30.5 51.5 4712 29.3 52.3 5374 AVE 28.2 67.7 4931 26.6 58.3 6485

EXAMPLE 8

The ball of Example 7-2 was compared to a number of competitive products in distance testing using a driving machine in which the ball was struck with a club. The results are shown on Table 29 below. The distance test shows that Example 7-2 is about the same distance as the Z-balata 90 control and longer than the Titleist HP-2 Tour (soft covered two-piece) and Titleist Tour Balata 100 ball (Balata covered wound ball). The other balls that were tested include the Maxfli (Dunlop) XS100, Maxfli (Dunlop) XF100, and the GIGA Top-Flite golf ball sold by Spalding in Japan. In Table 29, the ball of Example 7-2 is the longest ball.

TABLE 29 Distance Report Test Number: 131951 Club Head Speed (fps): 157.35 Club Name: TFT 10.5 DEG MW No. Balls/Type: 10 (DRIVER) Average Test Conditions: Launch Angles (Deg.): 9.6 Ball Speed (fps): 217.8 Spin Rate (rpm): 3390 Turf Condition: FIRM Wind (mph/dir): 2.55 135.20 Temp./RH (deg/%): 0.61 91.59 P-Bar (mbar): 1015 Car Ctr T Ball Type Traj Ptime Carry Diff Dev Roll T Dist Diff HP2TOUR 8.7 6.0 230.4 −4.1 3.0 9.9 240.3 −4.3 ZB90 9.0 6.1 231.8 −2.7 5.4 9.1 241.0 −3.6 GIGA 8.8 6.0 234.5 0.0 5.7 10.2 244.6 0.0 Example 7-2 8.3 5.9 229.6 −4.9 3.8 11.1 240.7 −3.9 Titleist Tour Balata 100 9.2 6.2 229.2 −5.3 7.8 7.8 236.9 −7.7 Test Number: 0203963 Club Head Speed (fps): 126.18 Club Name: TFT 5 IRON No. Balls/Type: 12 Average Test Conditions: Launch Angles (Deg.): 14 Ball Speed (fps): 180.1 Spin Rate (rpm): 5424 Turf Condition: FIRM Wind (mph/dir): 6.23 171.38 Temp./RH (deg/%): 62.20 98.16 P-Bar (mbar): 1015 Car Ctr T Ball Type Traj Ptime Carry Diff Dev Roll T Dist Diff HP2TOUR 25.3 6.0 156.0 −7.4 −3.0 1.5 157.5 −9.5 ZB90 25.2 6.0 157.1 −6.3 −3.3 2.2 159.3 −7.7 GIGA 25.0 6.0 162.2 −1.2 −3.1 2.9 165.1 −1.9 Example 7-2 23.5 6.0 163.4 0.0 −3.3 3.7 167.0 0.0 Titleist Tour Balata 100 23.9 6.0 158.7 −4.7 −2.3 2.5 161.2 −5.8 ZB 100 26.1 6.0 155.6 −7.8 −4.5 2.0 157.6 −9.4 XS 100 23.9 6.0 161.3 −2.3 −5.6 2.6 163.9 −3.1 XF 100 24.5 6.0 152.0 −11.4 −6.2 1.6 153.7 −13.3

EXAMPLE 9

A number of golf ball cores having the following formulation were made, as set forth in Table 30:

TABLE 30 PARTS High-cis polybutadiene 100 Zinc oxide 30 Core regrind 16 Zinc stearate 16 Zinc diacrylate 21 Peroxide (231 xl) 0.9 The cores had a diameter of 1.470″, a weight of 32.5 g, a PGA compression of 57 and a COR of 0.768.

The cores were divided into four sets and each set was covered with one of the mantle formulations shown below on Table 31.

TABLE 31 MANTLE FORMULATIONS Mantle Type A B C D (control) Surlyn 8940 (g) 656 880 1610 — Surlyn 9910 (g) 1964 2180 535 — Surlyn 8120 (g) 300 160 475 — Surlyn 8320 (g) 700 400 1000 — Iotek 7030 (g) 380 380 380 — Iotek 1002 (g) — — — 2000 Iotek 1003 (g) — — — 2000 The mantle covered cores had the following physical properties:

TABLE 32 MANTLE-COVERED CORES A B C D Size (Pole) (Inches) 1.577 1.576 1.572 1.573 Weight (g) 38.6 38.5 38.3 38.4 PGA Compression 71 74 70 76 COR .7795 .7831 .7768 .7946 Std. Dev. COR .0051 .0026 .0016 .0012 Shore C 92 94 90 97 Shore D 62 65 61 70 Each set of mantle-covered cores was divided into three subsets and a cover layer having one of the cover formulations shown on Table 33 was formed over the mantled cores. The “whitener package” on Table 33 has the same formulation as that shown above on Table 27.

TABLE 33 COVER FORMULATIONS Cover Type X Y Z Iotek 7520 (g) 1660 1480 1300 Iotek 7510 (g) 1660 1480 1300 Iotek 8000 (g) 304 664 1024 Iotek 7030 (g) 282 282 282 Whitener package (g) 94 94 94 The balls had the mantle and cover combinations and properties shown below on Table 34.

TABLE 34 BALL PROPERTIES Example No. 9-1 9-2 9-3 9-4 9-5 9-6 9-7 9-8 9-9 9-10 9-11 9-12 Mantle A A A B B B C C C D D D Cover X Y Z X Y Z X Y Z X Y Z Size (inch) 1.6820 1.6810 1.6820 1.6820 1.6820 1.6820 1.6820 1.6820 1.6820 1.6820 1.6820 1.6820 Weight (g) 45.68 45.57 45.58 45.77 45.62 45.58 45.63 45.58 45.48 45.67 45.65 45.57 PGA Comp. 73.5 74.3 74.7 77.4 76.7 76.3 70.8 71.9 73.3 79.5 80 82.5 COR .7639 .7665 .7680 .7701 .7703 .7704 .7607 .7630 .7661 .7771 .7798 .7839 Std. Dev. COR .0041 .0027 .0037 .0077 .0034 .0023 .0037 .0030 .0028 .0034 .0028 .0020 Shore C 71 76 81 71 76 81 70 76 80 71 76 81 Shore D 46 50 53 46 50 53 46 49 52 47 51 53 Ball 9–10 was the control.

The results from Table 34 demonstrate that a multi-layer ball having a mantle hardness of 60D or greater (Ex. 9-7,9-8, 9-9), and preferably 63D (Ex. 9-1,9-2, 903) or greater give a ball having a COR of at least 0.761 (Ex. 9-7) and while a harder mantle (Ex. 9-4,9-5, 9-6,9-10, 9-11, 9-12) will generally give higher COR, the mantle also contributes to a harder PGA compression. Versus the control ball (Ex. 9-10) it is demonstrated that softer compressions can be obtained with slightly softer mantles while maintaining a good COR. Likewise versus the control, higher COR balls may be designed (Ex. 9-11, 9-12) that still have a relatively soft compression for good feel.

EXAMPLE 10

A number of golf balls were made having the core and cover formulations and the physical properties shown on Tables 35 and 36. The balls of Examples 10-1, 10-2 and 10-5 are part of the invention. The balls of Examples 10-3, 10-4 and 10-6 are controls based upon the cover layer chemistry of comparative Example 2 of U.S. Pat. No. 5,586,950. The balls of Example 10-4 are replicas of comparative Example 2 of U.S. Pat. No. 5,586,950.

For all of the balls, the cores were molded and centerless ground to the appropriate size. The mantles of Examples 10-1 to 10-4 were injection molded in a 1.63″ injection mold. The mantles for the balls of Examples 10-5 and 10-6 also were injection molded. All of the outer cover layers were injection molded.

TABLE 35 EX. EX. EX. EX. EX. EX. 10-1 10-2 10-3 10-4 10-5 10-6 Core Data CoreType (see A A A A B B Table 36) Core Size (in.) 1.50 1.50 1.50 1.50 1.47 1.47 Mantle Data Ingredients phr phr phr phr phr phr Iotek 1002 50 — 50 — 50 50 Iotek 1003 50 — 50 — 50 50 Surlyn 9910 — 50 — 50 — — Surlyn 8940 — 35 — 35 — — Surlyn 8920 — 15 — 15 — — TiO₂ 2 2 2 2 — — Diameter (in.) 1.625 1.625 1.625 1.625 1.57 1.57 Thickness (in.) 0.063 0.063 0.063 0.063 0.050 0.050 Shore C/D 97/70 96/68 97/70 96/68 97/70 97/70 Hardness (measured on ball) Cover Data Cover Type (see #1 #1 #2 #2 #1 #2 Table 36) Size (in.) 1.70 1.70 1.70 1.70 1.68 1.68 Thickness 0.038 0.038 0.038 0.038 0.055 0.055 Shore C/D 75/49 75/49 84/57 83/57 72/48 83/56 Hardness (measured on ball) Compression 63 66 60 63 83 80 (Riehle) COR 800 795 805 798 779 787

TABLE 36 Core Formulations Cover Formulations Materials (phr) A B Materials (phr) #1 #2 BR 1220 73 70 Iotek 8000 8.5 — (High cis polybutadiene) Taktene 220 27 30 Iotek 7510 41 — (High cis polybutadiene) Zinc Oxide 22.3 31.5 Iotek 7520 41 — TG Regrind 10 16 Masterbatch C 9.5 — Zinc Stearate 20 16 Surlyn 1557 — 10 Zinc Diacrylate 26 20 Surlyn 1855 — 20 Masterbatch A 0.15 — Surlyn 8265 — 20 Masterbatch B — 0.15 Surlyn 8269 — 50 Luperco 231 XL 0.9 0.9 TiO₂ — 2 peroxide

EXAMPLE 11

A number of golf balls were made with mantles comprising a blend of polycarbonate and metallocene catalyzed polyolefin.

Cores having the formulation shown below on Table 39 were obtained and covered with a mantle layer formed from 83 parts by weight of Lexan ML 5776-7539 (GE) and 17 parts by weight of a maleic anhydride modified metallocene catalyzed polyolefin obtained from Exxon Chemical Co. and designated by Exxon as MDX-96-2. According to Exxon, MDX-96-2 contains 1.7 wt % maleic anhydride. This material was added as an impact modifier. The mantles were then covered with the same cover formulation as was used in Examples 7-3 and 7-4. The results are shown below on Table 39.

EXAMPLE 12

A number of golf balls were made using a nylon-ionomer graft copolymer as the mantle layer. The formulations and physical properties of the balls are shown below on Table 39.

EXAMPLE 13

The procedure of Example 11 was repeated with the exception that Lexan SP131OR-112 was used. This Lexan material was found to have a plaque Shore D hardness of 85 when tested in the lab. The plaque was stored at room temperature for several weeks before the Shore D hardness measurement was made.

EXAMPLE 14

The procedure of Example 11 was repeated with the exception of Capron 8351, a nylon-ionomer graft copolymer available from Allied-Signal, was used in the mantle layer in place of the polycarbonate and a different maeic anhydride modified metallocene catalyzed polyolefin was used, MDX 95-2. The formulations and physical properties of the balls are shown below on Table 39.

The properties of Capron 8351 are shown below on Table 37.

TABLE 37 CAPRON 8351 Flexurals at 23 C. Modulus, kpsi 235 Strength, kpsi 9.7 Notched Izod at 23 C., ft-lb/in 22.9 Failure Mode NB at −40 C., ft-leb/in 4.9 Failure Mode CB Drop Weight at 23 C. Impact Strength, ft-lbs 148 Failure Mode D Impact Strength, −40 C. Failure Mode Tensiles at 23 C. Strength at Break, kpsi 9.4 Strength at Yield, kpsi 7.3 Yield Elongation  3% Ultimate Elongation 277%

EXAMPLE 15

The procedure of Example 14 was repeated with the exception that Capron Ultratough, also known as Capron XA-2571, was used in place of Capron 8351. The properties of Capron XA-2571 are shown below on Table 38.

TABLE 38 CAPRON XA-2571 Flexurals at 23 C. Modulus, kpsi 240 Strength, kpsi 9.7 Notched Izod at 23 C, ft-lb/in 20 Failure Mode NB at −40 C., ft-lb/in 20.0 Failure Mode CB Drop Weight at 23 C. Impact Strength, ft-lbs 114 Failure Mode D Impact Strength, −40 C. 160 Failure Mode D Tensiles at 23 C. Strength at Break, kpsi 8.4 Strength at Yield, kpsi 6.9 Yield Elongation  7% Ultimate Elongation 200%

TABLE 39 Chemical Component EXAMPLE 11 EXAMPLE 12 EXAMPLE 13 EXAMPLE 14 Core Data Size 1.47″ 1.47″ 1.47″ 1.47″ Weight 32.7 g 32.7 g 32.7 g 32.7 g PGA Compression 78 78 78 78 COR (× 1000) 764 764 764 764 Composition (pph) High cis 100 100 100 100 polybutadiene Zinc oxide 6 6 6 6 Core regrind 10 10 10 10 Zinc Stearate 20 20 20 20 Zinc Diacrylate 20.5 20.5 20.5 20.5 Initiator 0.9 0.9 0.9 0.9 Inner Cover Layer Size 1.64″ 1.64″ 1.64″ 1.64″ Weight (g) 39.2 g 39.2 g 38.7 39.7 PGA Compression 95 97 96 97 COR (× 1000) 636 748 605 771 Thickness .100″ .100″ .100″ .100″ Hardness (Shore C) 95 98 95 95 (Shore D) 80 78 75 70 Composition (wt %) MDX 96-2 17% 17% — — MDX 95-2 — — 17% 17% LN SP131OR-112 — 83% — — LN ML 5776–7539 83% — — — CAPRON 8351 — — 83% — CAPRON XA 2571 — — — 83% Outer Cover Layer Hardness (Shore C/D) 71/46 71/46 71/46 71/46 Thickness 0.055″ 0.055″ 0.055″ 0.055″ Composition (wt %) Iotek 7510 42% 42% 42% 42% Iotek 7520 42% 42% 42% 42% Iotek 7030 7.3%  7.3%  7.3%  7.3%  Iotek 8000 8.7%  8.7%  8.7%  8.7%  Whitener Package Unitane 0-110  2.3 phr  2.3 phr  2.3 phr  2.3 phr Eastobrite OB1 0.025 phr 0.025 phr 0.025 phr 0.025 phr Ultra Marine Blue 0.042 phr 0.042 phr 0.042 phr 0.042 phr Santanox R 0.004 phr 0.004 phr 0.004 phr 0.004 phr Final Ball Data Size 1.73″ 1.73″ 1.73″ 1.73″ Weight 46.7 g 46.7 g 46.3 g 46.2 g PGA Compression 93 94 100 95 COR (× 1000) 746 719 672 753

EXAMPLE 16

A series of trial were conducted in which various preferred embodiment golf ball cores and corresponding mantle layers were produced in accordance with the present invention. These are summarized below in Tables 40–45. Tables 40–42 are for a first batch of cores and mantles, and Tables 43–45 are for a second batch of cores and mantles.

TABLE 43 RIM Center Compound BATCH MATERIAL PHR Specific Gravity Volume (mm) Volume (%) WEIGHT (g) BCP-820 40.00 0.910 43.956 31.23 320.00 Neo Cis 60 30.00 0.910 32.967 23.42 240.00 Neo Cis 40 30.00 0.910 32.967 23.42 240.00 ZINC OXIDE 22.65 5.570 4.066 2.89 181.20 Zn Stearate 16.00 1.090 14.679 10.43 128.00 ZDA 23.00 2.100 10.952 7.78 184.00 color-grey 0.40 1.400 0.286 0.20 3.20 Trig. 42-40B 1.25 1.400 0.893 0.63 10.00 TOTALS 163.30 1.1602 140.766 100.000 1306.400 NOTES mold in production dash 4 cavities (for 1.545″ dia cores) slug weight. = 42.3–43.3 grams glebar to 1.48″ diameter target glebarred properties: size: 1.48″ dia. weight 32.15 grams Riehle compression: 115 * once target properties are met, 18 doz. glebarred centers were made. Compound specific gravity = 1.1601 Batch factor = 8.00 Polymer Volume = 78.07%

TABLE 44 Center Glebarred Data Size pole = 1.478″ diameter off equator = 1.479″ diameter Weight 32.1 grams Comp. 45 PGA COR  .7878 Shore D 45 peak Rebound 85.5

TABLE 45 Mantled Data Mantle Mtl Surlyn 8140/6120 @ 50:50 (by weight) Mantle prep. Glebar & chlorination dip Mantle size 1.58″ diameter Weight 37.9 grams Comp. 75 PGA Rebound 84 COR  .8097

TABLE 43 RIM Center Compound Specific Volume Volume BATCH MATERIAL PHR Gravity (mm) (%) WEIGHT BCP-820 40.00 0.910 43.956 31.23 320.00 Neo Cis 60 30.00 0.910 32.967 23.46 240.00 Neo Cis 40 30.00 0.910 32.967 23.46 240.00 ZINC OXIDE 21.29 5.570 3.822 2.72 170.32 Zn Stearate 16.00 1.090 14.679 10.45 128.00 ZDA 23.00 2.100 10.952 7.79 184.00 color-orange 0.40 1.400 0.286 0.20 3.20 Trig. 42-40B 1.25 1.400 0.893 0.64 10.00 TOTALS 161.94 1.1524 140.522 100.000 1295.520 Notes mold in production dash 4 cavities (for 1.545″ dia cores) slug weight = 42.15–43.15 grams glebar to 1.51″ diameter target glebarred properties: size: 1.51″ dia. weight: 34.0 grams Riehle comp.: 115 *once target properties are met, 18 doz. glebarred centers were made. Compound specific gravity = 1.1524 Batch factor = 8.00 Polymer Vol. = 78.20%

TABLE 44 Center Glebarred Data Size pole = 1.511″ diameter off equator = 1.512″ diameter Weight 34.0 grams Comp. 44 PGA COR  .7856 Shore D 46 peak Rebound 85.9

TABLE 45 Mantled Data Mantle Mtl Surlyn 8140/6120 @ 50:50 (by weight) Mantle prep. Glebar & chlorination dip Mantled size 1.61″ diameter Weight 40 grams Comp. 73 PGA Rebound 85 COR  .8103 Shore D 68 Thickness 0.050″

EXAMPLE 17

Another series of trials were carried out in which golf balls having RIM polyurethane covers were produced in accordance with the present invention. These are summarized in Table 46 below:

TABLE 46 RIM Balls made @ Isotherm, 4/99 - 1st trial w/retractable pin mold CENTER, MANTLED CORE, BALL PHYSICAL PROPERTY/SPIN SUMMARY (PGA) (PGA) (PGA) cen- cen- cen- Jun. 7, 1999 ter center ter center ter core cor core core core ball ball Ball ball group code size weight comp cor reb size weight comp. cor reb. pole eq. weight comp. RIM. 0 1.51 34.0 42.3 0.7856 85.9 1.61 40.0 72.5 0.8103 85.4 1.6896 1.6900 45.88 79 035″ cover RIM. G 1.48 32.1 44.6 0.7878 85.5 1.58 37.9 74.7 0.8097 84.4 1.6877 1.6880 45.61 80 050″ cover Strata con- 1.47 — — — — 1.57 — — — — 1.6839 1.6834 45.53 71 Tour trol Prof 90 COVER (PGA) HARDNESS 9 iron Jun. 7, 1999 Ball ball ball dimples Moment cut scuff 9 iron launch group cor reb. ball plaque dura (2) (5) of Inertia (3) (4) spin angle RIM. 0.7992 78.3 56.3 40.2 140 D343C 0.4513 1 3 8542 27.3 035″ cover RIM. 0.7927 76.2 50.7 40.2 253 D343C 0.4480 1 3 9082 27.5 050″ cover Strata 0.7877 76.7 46.6 34.3 — D253 0.4383 1.5 4 9101 26.8 Tour Prof. 90 NOTES: center size based on 12 centers (all sizes are in inch units) center wt. based on 12 centers center comp. based on 12 centers center rebound based on 8 centers center COR based on 6 centers core size based on 12 cores core wt. based on 12 cores core comp. based on 12 cores core rebound based on 6 cores core COR based on 12 cores ball sizes based on 12 balls ball wt. based on 12 balls ball comp. based on 12 balls ball rebound based on 12 balls ball COR based on 12 balls 1.48″ center compound = Table 39 data, 45 Shore D peak 1.51″ center compound = Table 42 data, 46 Shore D peak Mantle material = Surlyn 8140/6120 @ 50–50 (1) hardness measured using Durotronic 2000 system; RIM plaque was 1 piece, 130″ thick (Bayer's MP 10000); Strata Tour Pro. Plaque was .120″ thick, 2 ply, Part No. BOO361 (gamma'd @ 40 KGYS) (2) ball durability based on a 4 clear balls each; all balls hit in barrel #5 (new score plate); all failures are cover-to-core adhesion failures; 0 breakdown - 1 @ 80 (pins), 1 @ 80 (random), 1 @ 150 (random), 1 @ 250 (pins); G breakdown - 1 @ 90 (pins), 2 @ 270 (pins), 1 @ 380 (cut in cover) - all groups ambient conditioned at least 2 weeks after molding prior to durability testing (3) cut based on a ranking of 1 to 6, 1 being the best (full height test) (4) scuff based on a ranking from 1–6, 1 being the best (5) cavities were coated with semi-permanent unicore release . . . didn't release well (approx. 40 shots worth) ball data based on painted balls using TCL epoxy white 6315/6316/6317: Urethane White 6318/6319/6320, both @ 120 gr. Wet with a 16 hr. Dry @ 100–105 F. in-between; std. Prod. SRC top coat Moment of Inertia Units are oz · in: paint adhesion ok for O & G balls: cracking observed mainly on G balls above were pressure blasted for 10 mins. @ ABS using 150 mesh white alum. oxide; paint cracking slightly less on pressure blasted balls versus brush tumble (adhesion ok on brush tumbled balls as well)

EXAMPLE 18

A polybutadiene golf ball core having a diameter of 1.545 inches, a PGA compression of about 65 and a coefficient of restitution of about 0.770 was obtained. A dimpled cover having a thickness of 0.0675 inches was reaction injection molded over the core. The cover comprised Bayflex MP 10000 resin (Bayer). The resulting ball had a PGA compression of 78, a COR of 0.720 and a Shore D cover hardness of 39.

EXAMPLE 19

A polybutadiene golf ball center having a diameter of 1.48 inches, a PGA compression of about 45, and a coefficient of restitution (COR) of about 0.788 was obtained. A 0.050 inch thick mantle layer was then injection molded over the center, made from a high acid thermoplastic ionomer material. The mantled core diameter was 1.58 inches, its PGA compression was about 75, and its COR was about 0.810. A dimpled cover having a thickness of about 0.050 inches was reaction injection molded over the mantled core. The cover was comprised of Bayer's Bayflex MP 10000 resin. The setting time of the mixed resin was about 4.5 seconds and the mold release time was about 20 seconds. The isocyanate tank temperature was about 115° F. and the polyol tank temperature was about 138° F. The mold temperature was about 157° F. The resulting ball, after painting, had a pole diameter of about 1.6877 inches, an equator diameter of about 1.6880 inches, a weight of about 45.61 grams, a PGA compression of about 80, a COR of about 0.793, a moment of inertia of about 0.448 oz-in², a drop rebound (based on a 100 inches drop) of about 76 inches, and a Shore D (peak) hardness of about 40 (measured on a 0.130 inch thick plaque of MP 10000).

EXAMPLE 20

A polybutadiene golf ball center having a diameter of 1.51 inches, a PGA compression of about 42, and a coefficient of restitution (COR) of about 0.786 was obtained. A 0.050 inch thick mantle layer was then injection molded over the center, made from a high acid thermoplastic ionomer material. The mantled core diameter was 1.61 inches, its PGA compression was about 73, and its COR was about 0.810. A dimpled cover having a thickness of about 0.035 inches was reaction injection molded over the mantled core. The cover was comprised of Bayer's Bayflex MP 10000 resin. The setting time of the mixed resin was about 4.5 seconds and the mold release time was about 20 seconds. The isocyanate tank temperature was about 115° F. and the polyol tank temperature was about 138° F. The mold temperature was about 156° F. The resulting ball, after painting, had a pole diameter of about 1.6896 inches, an equator diameter of about 1.6900 inches, a weight of about 45.68 grams, a PGA compression of about 79, a COR of about 0.799, a moment of inertia of about 0.451 oz-in², a drop rebound (based on a 100 inches drop) of about 78 inches, and a Shore D (peak) hardness of about 40 (measured on a 0.130 inch thick plaque of MP 10000).

The invention has been described with reference to the preferred embodiment. Obviously, modifications and alterations will occur to others upon reading and understanding the proceeding detailed description. It is intended that the invention be construed as including all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof. 

1. A golf ball comprising: a core; an inner cover layer disposed on the core, the inner cover layer having a Shore D hardness of at least 60, and an outer cover layer disposed on the inner core layer, wherein the outer cover layer comprises a reaction product of one or more reactive components selected from the group consisting of i) polyether-polyols, polyester-polyols, polyamine, and materials with an active hydrogen, and ii) one or more isocyanate-containing constituents, and wherein the outer cover layer is comprised of a relatively soft, low modulus material having a flexural modulus of from about 1,000 psi to about 10,000 psi.
 2. The golf ball of claim 1, wherein the golf ball exhibits a PGA compression of 100 or less and a coefficient of restitution of at least 0.750.
 3. The golf ball according to claim 1, wherein the outer cover layer has a Shore D hardness of less than
 53. 4. The golf ball according to claim 1, wherein the inner cover layer comprises of thermoplastic material.
 5. The golf ball according to claim 1, wherein the inner cover layer comprises an ionomer resin.
 6. The golf ball according to claim 1, wherein the inner cover layer has a Shore D hardness of from about 60 to about
 85. 7. The golf ball according to claim 1, wherein the outer cover layer has a Shore D hardness of from about 30 to about
 50. 8. The golf ball according to claim 1, wherein the inner cover layer comprises at least one member selected from the group consisting of polycarbonates, reaction-injection-molded polyurethanes, styrene-butadiene elastomers and combinations thereof.
 9. The golf ball according to claim 1, wherein the inner cover layer has a thickness of from about 0.01 to about 0.15 inches and the outer cover layer has a thickness of from about 0.01 to about 0.15 inches.
 10. The golf ball according to claim 1, wherein the core is selected from the group consisting of a solid core and a liquid filled core.
 11. A golf ball comprising: a core, a first inner cover layer formed about said core, a second inner cover layer formed about said first inner cover layer, said second inner cover layer including at least 50 weight percent of at least one material selected from the group consisting of ionomer resins, polycarbonates, reaction-injection-molded polyurethanes, styrene-butadiene elastomers and combinations thereof, and an outer cover layer formed over the second inner cover layer, the outer cover layer comprising a reaction product of one or more reactive components selected from the group consisting of i) polyether-polyols, polyester-polyols, polyamine, and materials with an active hydrogen, and ii) one or more isocyanate-containing constituents, the golf ball having a PGA compression of 100 or less and a coefficient of restitution of at least 0.750, and wherein the outer cover layer is comprised of a relatively soft, low modulus material having a flexural modulus of from about 1,000 psi to about 10 ,000 psi.
 12. The golf ball according to claim 11, wherein the second inner cover material is thermoplastic.
 13. The golf ball according to claim 11, wherein the second inner cover material is a thermoset.
 14. The golf ball according to claim 11, wherein the second inner cover material layer comprises a styrene-butadiene elastomer.
 15. The golf ball of claim 11, wherein the outer cover layer has a Shore D hardness of less than
 53. 16. The golf ball according to claim 15, wherein the outer cover layer has a Shore D hardness of from about 30 to about
 50. 